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Richard H. Myers, PhD - Publications

Affiliations: 
Neurology & Medicine Boston University, Boston, MA, United States 
Area:
http://www.researchprofiles.collexis.com/jad/expert.asp?u_id=145
Website:
http://www.bumc.bu.edu/neurology/clinicalfaculty/myers/
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Year Citation  Score
2024 Nazeen S, Wang X, Zielinski D, Lam I, Hallacli E, Xu P, Ethier E, Strom R, Zanella CA, Nithianandam V, Ritter D, Henderson A, Saurat N, Afroz J, Nutter-Upham A, ... ... Myers RH, et al. Deep sequencing of proteotoxicity modifier genes uncovers a Presenilin-2/beta-amyloid-actin genetic risk module shared among alpha-synucleinopathies. Biorxiv : the Preprint Server For Biology. PMID 38496508 DOI: 10.1101/2024.03.03.583145  0.314
2021 Lai D, Alipanahi B, Fontanillas P, Schwantes-An TH, Aasly J, Alcalay RN, Beecham GW, Berg D, Bressman S, Brice A, Brockman K, Clark L, Cookson M, Das S, Van Deerlin V, ... ... Myers RH, et al. Genome-wide association studies of LRRK2 modifiers of Parkinson's disease. Annals of Neurology. PMID 33938021 DOI: 10.1002/ana.26094  0.691
2020 Raghunathan R, Hogan JD, Labadorf A, Myers RH, Zaia J. A glycomics and proteomics study of aging and Parkinson's disease in human brain. Scientific Reports. 10: 12804. PMID 32733076 DOI: 10.1038/S41598-020-69480-3  0.738
2019 Ellis N, Tee A, McAllister B, Massey T, McLauchlan D, Stone T, Correia K, Loupe J, Kim KH, Barker D, Hong EP, Chao MJ, Long JD, Lucente D, Vonsattel JPG, ... ... Myers RH, et al. Genetic Risk Underlying Psychiatric and Cognitive Symptoms in Huntington's Disease. Biological Psychiatry. PMID 32087949 DOI: 10.1016/J.Biopsych.2019.12.010  0.311
2019 Agus F, Crespo D, Myers RH, Labadorf A. The caudate nucleus undergoes dramatic and unique transcriptional changes in human prodromal Huntington's disease brain. Bmc Medical Genomics. 12: 137. PMID 31619230 DOI: 10.1186/S12920-019-0581-9  0.722
2019 Lee J, Correia K, Loupe J, Kim K, Barker D, Hong EP, Chao MJ, Long JD, Lucente D, Vonsattel JPG, Pinto RM, Elneel KA, Ramos EM, Mysore JS, Gillis T, ... ... Myers RH, et al. CAG Repeat Not Polyglutamine Length Determines Timing of Huntington’s Disease Onset Cell. 178. PMID 31398342 DOI: 10.1016/J.Cell.2019.06.036  0.379
2018 Wyss AB, Sofer T, Lee MK, Terzikhan N, Nguyen JN, Lahousse L, Latourelle JC, Smith AV, Bartz TM, Feitosa MF, Gao W, Ahluwalia TS, Tang W, Oldmeadow C, Duan Q, ... ... Myers RH, et al. Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function. Nature Communications. 9: 2976. PMID 30061609 DOI: 10.1038/S41467-018-05369-0  0.677
2018 Hui KY, Fernandez-Hernandez H, Hu J, Schaffner A, Pankratz N, Hsu NY, Chuang LS, Carmi S, Villaverde N, Li X, Rivas M, Levine AP, Bao X, Labrias PR, Haritunians T, ... ... Myers RH, et al. Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's disease. Science Translational Medicine. 10. PMID 29321258 DOI: 10.1126/Scitranslmed.Aai7795  0.383
2018 Khan RR, Altmann A, Napolioni V, Kim Y, Guerreiro R, Bras JT, Carmona S, Pereira M, Santana I, Hardy J, Mead S, Cruchaga C, Fernandez MV, Holstege H, Flier WMVd, ... ... Myers R, et al. P4-240: Stop-Gain Variant In Microglia-Expressed Gene Gmip Is Associated With Early-Onset Alzheimer'S Disease Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.07.061  0.389
2018 Bonner D, Nguyen D, Cochran JN, Partridge C, Roberts B, Myers R. P1-171: Mapping Enhancer Regions For Genes Associated With Neurodegenerative Diseases Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.06.175  0.367
2017 Labadorf A, Choi SH, Myers RH. Evidence for a Pan-Neurodegenerative Disease Response in Huntington's and Parkinson's Disease Expression Profiles. Frontiers in Molecular Neuroscience. 10: 430. PMID 29375298 DOI: 10.3389/Fnmol.2017.00430  0.765
2017 Reed ER, Latourelle JC, Bockholt JH, Bregu J, Smock J, Paulsen JS, Myers RH. MicroRNAs in CSF as prodromal biomarkers for Huntington disease in the PREDICT-HD study. Neurology. PMID 29282329 DOI: 10.1212/Wnl.0000000000004844  0.647
2017 Lee JM, Chao MJ, Harold D, Abu Elneel K, Gillis T, Holmans P, Jones L, Orth M, Myers RH, Kwak S, Wheeler VC, MacDonald ME, Gusella JF. A modifier of Huntington's disease onset at the MLH1 locus. Human Molecular Genetics. 26: 3859-3867. PMID 28934397 DOI: 10.1093/Hmg/Ddx286  0.434
2017 Chao MJ, Gillis T, Atwal RS, Mysore JS, Arjomand J, Harold D, Holmans P, Jones L, Orth M, Myers RH, Kwak S, Wheeler VC, MacDonald ME, Gusella JF, Lee JM. Haplotype-based stratification of Huntington's disease. European Journal of Human Genetics : Ejhg. PMID 28832564 DOI: 10.1038/Ejhg.2017.125  0.416
2017 Neueder A, Landles C, Ghosh R, Howland D, Myers RH, Faull RLM, Tabrizi SJ, Bates GP. The pathogenic exon 1 HTT protein is produced by incomplete splicing in Huntington's disease patients. Scientific Reports. 7: 1307. PMID 28465506 DOI: 10.1038/S41598-017-01510-Z  0.363
2017 Choi SH, Labadorf AT, Myers RH, Lunetta KL, Dupuis J, DeStefano AL. Evaluation of logistic regression models and effect of covariates for case-control study in RNA-Seq analysis. Bmc Bioinformatics. 18: 91. PMID 28166718 DOI: 10.1186/S12859-017-1498-Y  0.689
2016 Wake C, Labadorf A, Dumitriu A, Hoss AG, Bregu J, Albrecht KH, DeStefano AL, Myers RH. Novel microRNA discovery using small RNA sequencing in post-mortem human brain. Bmc Genomics. 17: 776. PMID 27716130 DOI: 10.1186/S12864-016-3114-3  0.774
2016 Trinh J, Gustavsson EK, Vilariño-Güell C, Bortnick S, Latourelle J, McKenzie MB, Tu CS, Nosova E, Khinda J, Milnerwood A, Lesage S, Brice A, Tazir M, Aasly JO, Parkkinen L, ... ... Myers RH, et al. DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study. The Lancet. Neurology. PMID 27692902 DOI: 10.1016/S1474-4422(16)30203-4  0.693
2016 Nagle MW, Latourelle JC, Labadorf A, Dumitriu A, Hadzi TC, Beach TG, Myers RH. The 4p16.3 Parkinson Disease Risk Locus Is Associated with GAK Expression and Genes Involved with the Synaptic Vesicle Membrane. Plos One. 11: e0160925. PMID 27508417 DOI: 10.1371/Journal.Pone.0160925  0.814
2016 Nielson CM, Liu CT, Smith AV, Ackert-Bicknell CL, Reppe S, Johanna J, Wassel C, Register TC, Oei L, Alonso Lopez N, Oei EH, Parimi N, Samelson EJ, Nalls MA, Zmuda J, ... ... Myers RH, et al. Novel Genetic Variants are Associated With Increased Vertebral Volumetric BMD, Reduced Vertebral Fracture Risk, and Increased Expression of SCL1A3 and EPHB2. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. PMID 27476799 DOI: 10.1002/Jbmr.2913  0.67
2016 Labadorf A, Hoss AG, Lagomarsino V, Latourelle JC, Hadzi TC, Bregu J, MacDonald ME, Gusella JF, Chen JF, Akbarian S, Weng Z, Myers RH. Correction: RNA Sequence Analysis of Human Huntington Disease Brain Reveals an Extensive Increase in Inflammatory and Developmental Gene Expression. Plos One. 11: e0160295. PMID 27454300 DOI: 10.1371/journal.pone.0160295  0.775
2016 Soldner F, Stelzer Y, Shivalila CS, Abraham BJ, Latourelle JC, Barrasa MI, Goldmann J, Myers RH, Young RA, Jaenisch R. Parkinson-associated risk variant in distal enhancer of α-synuclein modulates target gene expression. Nature. PMID 27096366 DOI: 10.1038/Nature17939  0.721
2016 Hoss AG, Labadorf A, Beach TG, Latourelle JC, Myers RH. microRNA Profiles in Parkinson's Disease Prefrontal Cortex. Frontiers in Aging Neuroscience. 8: 36. PMID 26973511 DOI: 10.3389/Fnagi.2016.00036  0.807
2016 Kilpeläinen TO, Carli JF, Skowronski AA, Sun Q, Kriebel J, Feitosa MF, Hedman ÅK, Drong AW, Hayes JE, Zhao J, Pers TH, Schick U, Grarup N, Kutalik Z, Trompet S, ... ... Myers RH, et al. Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels. Nature Communications. 7: 10494. PMID 26833098 DOI: 10.1038/Ncomms10494  0.328
2016 Dumitriu A, Golji J, Labadorf AT, Gao B, Beach TG, Myers RH, Longo KA, Latourelle JC. Integrative analyses of proteomics and RNA transcriptomics implicate mitochondrial processes, protein folding pathways and GWAS loci in Parkinson disease. Bmc Medical Genomics. 9: 5. PMID 26793951 DOI: 10.1186/S12920-016-0164-Y  0.811
2016 Bates GP, Osborne GF, Ali N, Benjamin AC, Papadopoulou AS, Howland D, Tabrizi SJ, Faull RL, Myers RH, Landles C, Neueder A. B4 Detection of the aberrantly spliced exon 1 – intron 1 htt mRNA in HD patient post mortem brain tissue and fibroblast lines Journal of Neurology, Neurosurgery & Psychiatry. 87: A10.2-A10. DOI: 10.1136/Jnnp-2016-314597.35  0.309
2015 Labadorf A, Hoss AG, Lagomarsino V, Latourelle JC, Hadzi TC, Bregu J, MacDonald ME, Gusella JF, Chen JF, Akbarian S, Weng Z, Myers RH. RNA Sequence Analysis of Human Huntington Disease Brain Reveals an Extensive Increase in Inflammatory and Developmental Gene Expression. Plos One. 10: e0143563. PMID 26636579 DOI: 10.1371/Journal.Pone.0143563  0.793
2015 Dong X, Tsuji J, Labadorf A, Roussos P, Chen JF, Myers RH, Akbarian S, Weng Z. The Role of H3K4me3 in Transcriptional Regulation Is Altered in Huntington's Disease. Plos One. 10: e0144398. PMID 26636336 DOI: 10.1371/Journal.Pone.0144398  0.721
2015 Hoss AG, Lagomarsino VN, Frank S, Hadzi TC, Myers RH, Latourelle JC. Study of plasma-derived miRNAs mimic differences in Huntington's disease brain. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 26573701 DOI: 10.1002/Mds.26457  0.784
2015 Labadorf AT, Myers RH. Evidence of Extensive Alternative Splicing in Post Mortem Human Brain HTT Transcription by mRNA Sequencing. Plos One. 10: e0141298. PMID 26496077 DOI: 10.1371/Journal.Pone.0141298  0.716
2015 Correia K, Harold D, Kim KH, Holmans P, Jones L, Orth M, Myers RH, Kwak S, Wheeler VC, MacDonald ME, Gusella JF, Lee JM. The Genetic Modifiers of Motor OnsetAge (GeM MOA) Website: Genome-wide Association Analysis for Genetic Modifiers of Huntington's Disease. Journal of Huntington's Disease. 4: 279-84. PMID 26444025 DOI: 10.3233/Jhd-150169  0.365
2015 Lee JM, Kim KH, Shin A, Chao MJ, Abu Elneel K, Gillis T, Mysore JS, Kaye JA, Zahed H, Kratter IH, Daub AC, Finkbeiner S, Li H, Roach JC, Goodman N, ... ... Myers RH, et al. Sequence-Level Analysis of the Major European Huntington Disease Haplotype. American Journal of Human Genetics. 97: 435-44. PMID 26320893 DOI: 10.1016/J.Ajhg.2015.07.017  0.419
2015 Joshi PK, Esko T, Mattsson H, Eklund N, Gandin I, Nutile T, Jackson AU, Schurmann C, Smith AV, Zhang W, Okada Y, Stančáková A, Faul JD, Zhao W, Bartz TM, ... ... Myers RH, et al. Directional dominance on stature and cognition in diverse human populations. Nature. 523: 459-62. PMID 26131930 DOI: 10.1038/Nature14618  0.322
2015 Hoss AG, Labadorf A, Latourelle JC, Kartha VK, Hadzi TC, Gusella JF, MacDonald ME, Chen JF, Akbarian S, Weng Z, Vonsattel JP, Myers RH. miR-10b-5p expression in Huntington's disease brain relates to age of onset and the extent of striatal involvement. Bmc Medical Genomics. 8: 10. PMID 25889241 DOI: 10.1186/S12920-015-0083-3  0.774
2015 Bai G, Cheung I, Shulha HP, Coelho JE, Li P, Dong X, Jakovcevski M, Wang Y, Grigorenko A, Jiang Y, Hoss A, Patel K, Zheng M, Rogaev E, Myers RH, et al. Epigenetic dysregulation of hairy and enhancer of split 4 (HES4) is associated with striatal degeneration in postmortem Huntington brains. Human Molecular Genetics. 24: 1441-56. PMID 25480889 DOI: 10.1093/Hmg/Ddu561  0.787
2015 DiMucci D, Ivison R, Jenkins D, Dumitriu A, Labadorf A, Wake C, Benson G, Myers RH. Identifying allele specific expression in Parkinson's disease brain tissue F1000research. 4. DOI: 10.7490/F1000Research.1110302.1  0.8
2015 Lee JM, Wheeler VC, Chao MJ, Vonsattel JPG, Pinto RM, Lucente D, Abu-Elneel K, Ramos EM, Mysore JS, Gillis T, MacDonald ME, Gusella JF, Harold D, Stone TC, Escott-Price V, ... ... Myers RH, et al. Identification of Genetic Factors that Modify Clinical Onset of Huntington's Disease Cell. 162: 516-526. DOI: 10.1016/J.Cell.2015.07.003  0.402
2014 Nalls MA, Pankratz N, Lill CM, Do CB, Hernandez DG, Saad M, DeStefano AL, Kara E, Bras J, Sharma M, Schulte C, Keller MF, Arepalli S, Letson C, Edsall C, ... ... Myers RH, et al. Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease. Nature Genetics. 46: 989-93. PMID 25064009 DOI: 10.1038/Ng.3043  0.414
2014 Hoss AG, Kartha VK, Dong X, Latourelle JC, Dumitriu A, Hadzi TC, Macdonald ME, Gusella JF, Akbarian S, Chen JF, Weng Z, Myers RH. MicroRNAs located in the Hox gene clusters are implicated in huntington's disease pathogenesis. Plos Genetics. 10: e1004188. PMID 24586208 DOI: 10.1371/Journal.Pgen.1004188  0.776
2014 Hendricks AE, Dupuis J, Logue MW, Myers RH, Lunetta KL. Correction for multiple testing in a gene region. European Journal of Human Genetics : Ejhg. 22: 414-8. PMID 23838599 DOI: 10.1038/Ejhg.2013.144  0.339
2014 Jones L, Gusella J, MacDonald M, Wheeler V, Lee J, Myers R, Latourelle J, Harold D, Holmans P, Orth M, Kwak S. A03 Genetic Modifiers Affecting The Age At Motor Onset In Huntington’s Disease Journal of Neurology, Neurosurgery, and Psychiatry. 85. DOI: 10.1136/Jnnp-2014-309032.3  0.707
2013 Pichler I, Del Greco M F, Gögele M, Lill CM, Bertram L, Do CB, Eriksson N, Foroud T, Myers RH, Nalls M, Keller MF, Benyamin B, et al. Serum iron levels and the risk of Parkinson disease: a Mendelian randomization study. Plos Medicine. 10: e1001462. PMID 23750121 DOI: 10.1371/Journal.Pmed.1001462  0.38
2013 Ramos EM, Latourelle JC, Gillis T, Mysore JS, Squitieri F, Di Pardo A, Di Donato S, Gellera C, Hayden MR, Morrison PJ, Nance M, Ross CA, Margolis RL, Gomez-Tortosa E, Ayuso C, ... ... Myers RH, et al. Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onset. Neurogenetics. 14: 173-9. PMID 23644918 DOI: 10.1007/S10048-013-0364-Y  0.696
2013 Dumitriu A, Myers RH, McKee A, Seshadri S, Destefano A. P1-067: RNA-sequencing evaluation of fresh frozen and formaldehyde-fixed prefrontal cortex brain tissue for the study of Alzheimer's disease Alzheimer's & Dementia. 9: P177-P177. DOI: 10.1016/J.Jalz.2013.05.288  0.618
2012 Shulha HP, Crisci JL, Reshetov D, Tushir JS, Cheung I, Bharadwaj R, Chou HJ, Houston IB, Peter CJ, Mitchell AC, Yao WD, Myers RH, Chen JF, Preuss TM, Rogaev EI, et al. Human-specific histone methylation signatures at transcription start sites in prefrontal neurons. Plos Biology. 10: e1001427. PMID 23185133 DOI: 10.1371/Journal.Pbio.1001427  0.336
2012 Latourelle JC, Dumitriu A, Hadzi TC, Beach TG, Myers RH. Evaluation of Parkinson disease risk variants as expression-QTLs. Plos One. 7: e46199. PMID 23071545 DOI: 10.1371/Journal.Pone.0046199  0.811
2012 Hadzi TC, Hendricks AE, Latourelle JC, Lunetta KL, Cupples LA, Gillis T, Mysore JS, Gusella JF, MacDonald ME, Myers RH, Vonsattel JP. Assessment of cortical and striatal involvement in 523 Huntington disease brains. Neurology. 79: 1708-15. PMID 23035064 DOI: 10.1212/Wnl.0B013E31826E9A5D  0.65
2012 Wilk JB, Shrine NR, Loehr LR, Zhao JH, Manichaikul A, Lopez LM, Smith AV, Heckbert SR, Smolonska J, Tang W, Loth DW, Curjuric I, Hui J, Cho MH, Latourelle JC, ... ... Myers RH, et al. Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction. American Journal of Respiratory and Critical Care Medicine. 186: 622-32. PMID 22837378 DOI: 10.1164/Rccm.201202-0366Oc  0.785
2012 Ramos EM, Latourelle JC, Lee JH, Gillis T, Mysore JS, Squitieri F, Di Pardo A, Di Donato S, Hayden MR, Morrison PJ, Nance M, Ross CA, Margolis RL, Gomez-Tortosa E, Ayuso C, ... ... Myers RH, et al. Population stratification may bias analysis of PGC-1α as a modifier of age at Huntington disease motor onset. Human Genetics. 131: 1833-40. PMID 22825315 DOI: 10.1007/S00439-012-1205-Z  0.697
2012 Lee JH, Lee JM, Ramos EM, Gillis T, Mysore JS, Kishikawa S, Hadzi T, Hendricks AE, Hayden MR, Morrison PJ, Nance M, Ross CA, Margolis RL, Squitieri F, Gellera C, ... ... Myers RH, et al. TAA repeat variation in the GRIK2 gene does not influence age at onset in Huntington's disease. Biochemical and Biophysical Research Communications. 424: 404-8. PMID 22771793 DOI: 10.1016/J.Bbrc.2012.06.120  0.41
2012 Dumitriu A, Latourelle JC, Hadzi TC, Pankratz N, Garza D, Miller JP, Vance JM, Foroud T, Beach TG, Myers RH. Gene expression profiles in Parkinson disease prefrontal cortex implicate FOXO1 and genes under its transcriptional regulation. Plos Genetics. 8: e1002794. PMID 22761592 DOI: 10.1371/Journal.Pgen.1002794  0.823
2012 Dumitriu A, Moser C, Hadzi TC, Williamson SL, Pacheco CD, Hendricks AE, Latourelle JC, Wilk JB, Destefano AL, Myers RH. Postmortem Interval Influences α-Synuclein Expression in Parkinson Disease Brain. Parkinson's Disease. 2012: 614212. PMID 22530163 DOI: 10.1155/2012/614212  0.818
2012 Pankratz N, Beecham GW, DeStefano AL, Dawson TM, Doheny KF, Factor SA, Hamza TH, Hung AY, Hyman BT, Ivinson AJ, Krainc D, Latourelle JC, Clark LN, Marder K, Martin ER, ... ... Myers RH, et al. Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2. Annals of Neurology. 71: 370-84. PMID 22451204 DOI: 10.1002/Ana.22687  0.731
2012 Lill CM, Roehr JT, McQueen MB, Kavvoura FK, Bagade S, Schjeide BM, Schjeide LM, Meissner E, Zauft U, Allen NC, Liu T, Schilling M, Anderson KJ, Beecham G, Berg D, ... ... Myers RH, et al. Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. Plos Genetics. 8: e1002548. PMID 22438815 DOI: 10.1371/Journal.Pgen.1002548  0.735
2012 Lee JM, Gillis T, Mysore JS, Ramos EM, Myers RH, Hayden MR, Morrison PJ, Nance M, Ross CA, Margolis RL, Squitieri F, Griguoli A, Di Donato S, Gomez-Tortosa E, Ayuso C, et al. Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region. American Journal of Human Genetics. 90: 434-44. PMID 22387017 DOI: 10.1016/J.Ajhg.2012.01.005  0.422
2012 Lee JM, Ramos EM, Lee JH, Gillis T, Mysore JS, Hayden MR, Warby SC, Morrison P, Nance M, Ross CA, Margolis RL, Squitieri F, Orobello S, Di Donato S, Gomez-Tortosa E, ... ... Myers RH, et al. CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion. Neurology. 78: 690-5. PMID 22323755 DOI: 10.1212/Wnl.0B013E318249F683  0.342
2012 Sebastiani P, Solovieff N, Dewan AT, Walsh KM, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Hoh J, et al. Genetic signatures of exceptional longevity in humans. Plos One. 7: e29848. PMID 22279548 DOI: 10.1371/Journal.Pone.0029848  0.654
2012 Sebastiani P, Solovieff N, DeWan AT, Walsh KM, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Hoh J, et al. Example of 9 clusters of genetic risk profiles in centenarians of the discovery set and 3 similar clusters in replication sets 1 and 2. Plos One. DOI: 10.1371/Journal.Pone.0029848.G008  0.583
2011 Pankratz N, Dumitriu A, Hetrick KN, Sun M, Latourelle JC, Wilk JB, Halter C, Doheny KF, Gusella JF, Nichols WC, Myers RH, Foroud T, DeStefano AL. Copy number variation in familial Parkinson disease. Plos One. 6: e20988. PMID 21829596 DOI: 10.1371/Journal.Pone.0020988  0.824
2011 Sebastiani P, Solovieff N, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Perls TT. Retraction. Science (New York, N.Y.). 333: 404. PMID 21778381 DOI: 10.1126/science.333.6041.404-a  0.502
2011 Soldner F, Laganière J, Cheng AW, Hockemeyer D, Gao Q, Alagappan R, Khurana V, Golbe LI, Myers RH, Lindquist S, Zhang L, Guschin D, Fong LK, Vu BJ, Meng X, et al. Generation of isogenic pluripotent stem cells differing exclusively at two early onset Parkinson point mutations. Cell. 146: 318-31. PMID 21757228 DOI: 10.1016/J.Cell.2011.06.019  0.335
2011 Latourelle JC, Hendricks AE, Pankratz N, Wilk JB, Halter C, Nichols WC, Gusella JF, Destefano AL, Myers RH, Foroud T. Genomewide linkage study of modifiers of LRRK2-related Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 26: 2039-44. PMID 21661047 DOI: 10.1002/Mds.23781  0.799
2011 Dumitriu A, Pacheco CD, Wilk JB, Strathearn KE, Latourelle JC, Goldwurm S, Pezzoli G, Rochet JC, Lindquist S, Myers RH. Cyclin-G-associated kinase modifies α-synuclein expression levels and toxicity in Parkinson's disease: results from the GenePD Study. Human Molecular Genetics. 20: 1478-87. PMID 21258085 DOI: 10.1093/Hmg/Ddr026  0.828
2010 Speliotes EK, Willer CJ, Berndt SI, Monda KL, Thorleifsson G, Jackson AU, Lango Allen H, Lindgren CM, Luan J, Mägi R, Randall JC, Vedantam S, Winkler TW, Qi L, Workalemahu T, ... ... Myers RH, et al. Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nature Genetics. 42: 937-48. PMID 20935630 DOI: 10.1038/Ng.686  0.341
2010 Latourelle JC, Dybdahl M, Destefano AL, Myers RH, Lash TL. Estrogen-related and other disease diagnoses preceding Parkinson's disease. Clinical Epidemiology. 2: 153-70. PMID 20865113 DOI: 10.2147/Clep.S9621  0.77
2010 Lanoue AC, Dumitriu A, Myers RH, Soghomonian JJ. Decreased glutamic acid decarboxylase mRNA expression in prefrontal cortex in Parkinson's disease. Experimental Neurology. 226: 207-17. PMID 20832408 DOI: 10.1016/J.Expneurol.2010.09.001  0.687
2010 Sebastiani P, Solovieff N, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Perls TT. Genetic signatures of exceptional longevity in humans. Science (New York, N.Y.). 2010. PMID 20595579 DOI: 10.1126/Science.1190532  0.662
2010 Latourelle JC, Dybdahl M, Destefano AL, Myers RH, Lash TL. Risk of Parkinson's disease after tamoxifen treatment. Bmc Neurology. 10: 23. PMID 20385012 DOI: 10.1186/1471-2377-10-23  0.739
2009 Latourelle JC, Pankratz N, Dumitriu A, Wilk JB, Goldwurm S, Pezzoli G, Mariani CB, DeStefano AL, Halter C, Gusella JF, Nichols WC, Myers RH, Foroud T. Genomewide association study for onset age in Parkinson disease. Bmc Medical Genetics. 10: 98. PMID 19772629 DOI: 10.1186/1471-2350-10-98  0.84
2009 Feitosa MF, North KE, Myers RH, Pankow JS, Borecki IB. Evidence for three novel QTLs for adiposity on chromosome 2 with epistatic interactions: the NHLBI Family Heart Study. Obesity (Silver Spring, Md.). 17: 2190-5. PMID 19521348 DOI: 10.1038/Oby.2009.181  0.307
2009 Hendricks AE, Latourelle JC, Lunetta KL, Cupples LA, Wheeler V, MacDonald ME, Gusella JF, Myers RH. Estimating the probability of de novo HD cases from transmissions of expanded penetrant CAG alleles in the Huntington disease gene from male carriers of high normal alleles (27-35 CAG). American Journal of Medical Genetics. Part A. 149: 1375-81. PMID 19507258 DOI: 10.1002/Ajmg.A.32901  0.67
2009 Swami M, Hendricks AE, Gillis T, Massood T, Mysore J, Myers RH, Wheeler VC. Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onset. Human Molecular Genetics. 18: 3039-47. PMID 19465745 DOI: 10.1093/Hmg/Ddp242  0.379
2009 Laramie JM, Wilk JB, Williamson SL, Nagle MW, Latourelle JC, Tobin JE, Province MA, Borecki IB, Myers RH. Multiple genes influence BMI on chromosome 7q31-34: the NHLBI Family Heart Study. Obesity (Silver Spring, Md.). 17: 2182-9. PMID 19461589 DOI: 10.1038/Oby.2009.141  0.801
2009 Wilk JB, Chen TH, Gottlieb DJ, Walter RE, Nagle MW, Brandler BJ, Myers RH, Borecki IB, Silverman EK, Weiss ST, O'Connor GT. A genome-wide association study of pulmonary function measures in the Framingham Heart Study. Plos Genetics. 5: e1000429. PMID 19300500 DOI: 10.1371/Journal.Pgen.1000429  0.809
2009 Franceschini N, North KE, Arnett D, Pankow JS, Chung JH, Baird L, Leppert MF, Eckfeldt JH, Boerwinkle E, Gu CC, Lewis CE, Myers RH, Turner ST, Weder A, Kao WH, et al. The association of cell cycle checkpoint 2 variants and kidney function: findings of the Family Blood Pressure Program and the Atherosclerosis Risk In Communities study. American Journal of Hypertension. 22: 552-8. PMID 19265784 DOI: 10.1038/Ajh.2009.41  0.349
2009 Wu J, Pankow JS, Tracy RP, North KE, Myers RH, Feitosa ME, Province MA, Borecki IB. A QTL on 12q influencing an inflammation marker and obesity in white women: the NHLBI Family Heart Study. Obesity (Silver Spring, Md.). 17: 525-31. PMID 19238141 DOI: 10.1038/Oby.2008.556  0.307
2009 Ma D, Feitosa MF, Wilk JB, Laramie JM, Yu K, Leiendecker-Foster C, Myers RH, Province MA, Borecki IB. Leptin is associated with blood pressure and hypertension in women from the National Heart, Lung, and Blood Institute Family Heart Study. Hypertension. 53: 473-9. PMID 19204185 DOI: 10.1161/Hypertensionaha.108.118133  0.756
2009 Feitosa MF, Myers RH, Pankow JS, Province MA, Borecki IB. LIPC variants in the promoter and intron 1 modify HDL-C levels in a sex-specific fashion. Atherosclerosis. 204: 171-7. PMID 19101670 DOI: 10.1016/J.Atherosclerosis.2008.09.007  0.351
2009 Shi G, Gu CC, Kraja AT, Arnett DK, Myers RH, Pankow JS, Hunt SC, Rao DC. Genetic effect on blood pressure is modulated by age: the Hypertension Genetic Epidemiology Network Study. Hypertension. 53: 35-41. PMID 19029486 DOI: 10.1161/Hypertensionaha.108.120071  0.341
2009 Pankratz N, Wilk JB, Latourelle JC, DeStefano AL, Halter C, Pugh EW, Doheny KF, Gusella JF, Nichols WC, Foroud T, Myers RH. Genomewide association study for susceptibility genes contributing to familial Parkinson disease. Human Genetics. 124: 593-605. PMID 18985386 DOI: 10.1007/S00439-008-0582-9  0.815
2008 Latourelle JC, Sun M, Lew MF, Suchowersky O, Klein C, Golbe LI, Mark MH, Growdon JH, Wooten GF, Watts RL, Guttman M, Racette BA, Perlmutter JS, Ahmed A, Shill HA, ... ... Myers RH, et al. The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study. Bmc Medicine. 6: 32. PMID 18986508 DOI: 10.1186/1741-7015-6-32  0.803
2008 McNicoll CF, Latourelle JC, MacDonald ME, Lew MF, Suchowersky O, Klein C, Golbe LI, Mark MH, Growdon JH, Wooten GF, Watts RL, Guttman M, Racette BA, Perlmutter JS, Ahmed A, ... ... Myers RH, et al. Huntington CAG repeat size does not modify onset age in familial Parkinson's disease: the GenePD study. Movement Disorders : Official Journal of the Movement Disorder Society. 23: 1596-601. PMID 18649400 DOI: 10.1002/Mds.22186  0.733
2008 DeStefano AL, Latourelle J, Lew MF, Suchowersky O, Klein C, Golbe LI, Mark MH, Growdon JH, Wooten GF, Watts R, Guttman M, Racette BA, Perlmutter JS, Marlor L, Shill HA, ... ... Myers RH, et al. Replication of association between ELAVL4 and Parkinson disease: the GenePD study. Human Genetics. 124: 95-9. PMID 18587682 DOI: 10.1007/S00439-008-0526-4  0.825
2008 Tobin JE, Latourelle JC, Lew MF, Klein C, Suchowersky O, Shill HA, Golbe LI, Mark MH, Growdon JH, Wooten GF, Racette BA, Perlmutter JS, Watts R, Guttman M, Baker KB, ... ... Myers RH, et al. Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study. Neurology. 71: 28-34. PMID 18509094 DOI: 10.1212/01.Wnl.0000304051.01650.23  0.823
2008 Laramie JM, Wilk JB, Williamson SL, Nagle MW, Latourelle JC, Tobin JE, Province MA, Borecki IB, Myers RH. Polymorphisms near EXOC4 and LRGUK on chromosome 7q32 are associated with Type 2 Diabetes and fasting glucose; the NHLBI Family Heart Study. Bmc Medical Genetics. 9: 46. PMID 18498660 DOI: 10.1186/1471-2350-9-46  0.791
2008 Wilk JB, Laramie JM, Latourelle JC, Williamson S, Nagle MW, Tobin JE, Foster CL, Eckfeldt JH, Province MA, Borecki IB, Myers RH. NYD-SP18 is associated with obesity in the NHLBI Family Heart Study. International Journal of Obesity (2005). 32: 930-5. PMID 18317470 DOI: 10.1038/Ijo.2008.23  0.785
2008 Zhang Q, Lewis CE, Wagenknecht LE, Myers RH, Pankow JS, Hunt SC, North KE, Hixson JE, Jeffrey Carr J, Shimmin LC, Borecki I, Province MA. Genome-wide admixture mapping for coronary artery calcification in African Americans: the NHLBI Family Heart Study. Genetic Epidemiology. 32: 264-72. PMID 18200599 DOI: 10.1002/Gepi.20301  0.328
2008 Bielinski SJ, Pankow JS, Foster CL, Miller MB, Hopkins PN, Eckfeldt JH, Hixson J, Liu Y, Register T, Myers RH, Arnett DK. Circulating soluble ICAM-1 levels shows linkage to ICAM gene cluster region on chromosome 19: the NHLBI Family Heart Study follow-up examination. Atherosclerosis. 199: 172-8. PMID 18045607 DOI: 10.1016/J.Atherosclerosis.2007.10.006  0.398
2007 Bielinski SJ, Pankow JS, Miller MB, Hopkins PN, Eckfeldt JH, Hixson J, Liu Y, Register T, Myers RH, Arnett DK. Circulating MCP-1 levels shows linkage to chemokine receptor gene cluster on chromosome 3: the NHLBI family heart study follow-up examination. Genes and Immunity. 8: 684-90. PMID 17917677 DOI: 10.1038/Sj.Gene.6364434  0.352
2007 Dupré N, Rivière JB, Myers RH, Provencher P, Pourcher E, Emond F, Rouleau GA. LRRK2 is not a significant cause of Parkinson's disease in French-Canadians. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 34: 333-5. PMID 17803032 DOI: 10.1017/S0317167100006776  0.448
2007 Wheeler VC, Persichetti F, McNeil SM, Mysore JS, Mysore SS, MacDonald ME, Myers RH, Gusella JF, Wexler NS. Factors associated with HD CAG repeat instability in Huntington disease. Journal of Medical Genetics. 44: 695-701. PMID 17660463 DOI: 10.1136/Jmg.2007.050930  0.319
2007 Laramie JM, Wilk JB, DeStefano AL, Myers RH. HaploBuild: an algorithm to construct non-contiguous associated haplotypes in family based genetic studies. Bioinformatics (Oxford, England). 23: 2190-2. PMID 17586827 DOI: 10.1093/Bioinformatics/Btm316  0.783
2007 Litvan I, Chesselet MF, Gasser T, Di Monte DA, Parker D, Hagg T, Hardy J, Jenner P, Myers RH, Price D, Hallett M, Langston WJ, Lang AE, Halliday G, Rocca W, et al. The etiopathogenesis of Parkinson disease and suggestions for future research. Part II. Journal of Neuropathology and Experimental Neurology. 66: 329-36. PMID 17483689 DOI: 10.1097/Nen.0B013E318053716A  0.389
2007 Tobin JE, Cui J, Wilk JB, Latourelle JC, Laramie JM, McKee AC, Guttman M, Karamohamed S, DeStefano AL, Myers RH. Sepiapterin reductase expression is increased in Parkinson's disease brain tissue. Brain Research. 1139: 42-7. PMID 17270157 DOI: 10.1016/J.Brainres.2007.01.001  0.828
2007 Greenwood TA, Libiger O, Kardia S, Hanis C, Morrison AC, Gu CC, Rice T, Miller M, Turner ST, Myers RH, Grove J, Hsiao CF, Weder AB, Schork NJ. Comprehensive linkage and linkage heterogeneity analysis of 4344 sibling pairs affected with hypertension from the Family Blood Pressure Program. Genetic Epidemiology. 31: 195-210. PMID 17266112 DOI: 10.1002/Gepi.20202  0.369
2007 North KE, Franceschini N, Borecki IB, Gu CC, Heiss G, Province MA, Arnett DK, Lewis CE, Miller MB, Myers RH, Hunt SC, Freedman BI. Genotype-by-sex interaction on fasting insulin concentration: the HyperGEN study. Diabetes. 56: 137-42. PMID 17192475 DOI: 10.2337/Db06-0624  0.306
2007 Andresen JM, Gayán J, Djoussé L, Roberts S, Brocklebank D, Cherny SS, Cardon LR, Gusella JF, MacDonald ME, Myers RH, Housman DE, Wexler NS. The relationship between CAG repeat length and age of onset differs for Huntington's disease patients with juvenile onset or adult onset. Annals of Human Genetics. 71: 295-301. PMID 17181545 DOI: 10.1111/J.1469-1809.2006.00335.X  0.334
2007 Feitosa MF, Province MA, Heiss G, Arnett DK, Myers RH, Pankow JS, Hopkins PN, Borecki IB. Evidence of QTL on 15q21 for high-density lipoprotein cholesterol: the National Heart, Lung, and Blood Institute Family Heart Study (NHLBI FHS). Atherosclerosis. 190: 232-7. PMID 16529751 DOI: 10.1016/J.Atherosclerosis.2006.02.006  0.309
2006 Wilk JB, Tobin JE, Suchowersky O, Shill HA, Klein C, Wooten GF, Lew MF, Mark MH, Guttman M, Watts RL, Singer C, Growdon JH, Latourelle JC, Saint-Hilaire MH, DeStefano AL, ... ... Myers RH, et al. Herbicide exposure modifies GSTP1 haplotype association to Parkinson onset age: the GenePD Study. Neurology. 67: 2206-10. PMID 17190945 DOI: 10.1212/01.Wnl.0000249149.22407.D1  0.801
2006 Kishikawa S, Li JL, Gillis T, Hakky MM, Warby S, Hayden M, MacDonald ME, Myers RH, Gusella JF. Brain-derived neurotrophic factor does not influence age at neurologic onset of Huntington's disease. Neurobiology of Disease. 24: 280-5. PMID 16962786 DOI: 10.1016/J.Nbd.2006.07.008  0.559
2006 Zeng W, Gillis T, Hakky M, Djoussé L, Myers RH, MacDonald ME, Gusella JF. Genetic analysis of the GRIK2 modifier effect in Huntington's disease. Bmc Neuroscience. 7: 62. PMID 16959037 DOI: 10.1186/1471-2202-7-62  0.414
2006 Li JL, Hayden MR, Warby SC, Durr A, Morrison PJ, Nance M, Ross CA, Margolis RL, Rosenblatt A, Squitieri F, Frati L, Gómez-Tortosa E, García CA, Suchowersky O, Klimek ML, ... ... Myers RH, et al. Genome-wide significance for a modifier of age at neurological onset in Huntington's disease at 6q23-24: the HD MAPS study. Bmc Medical Genetics. 7: 71. PMID 16914060 DOI: 10.1186/1471-2350-7-71  0.566
2006 Wilk JB, Myers RH, Pankow JS, Hunt SC, Leppert MF, Freedman BI, Province MA, Ellison RC. Adrenergic receptor polymorphisms associated with resting heart rate: the HyperGEN Study. Annals of Human Genetics. 70: 566-73. PMID 16907703 DOI: 10.1111/J.1469-1809.2005.00258.X  0.614
2006 Avery CL, Freedman BI, Kraja AT, Borecki IB, Miller MB, Pankow JS, Arnett D, Lewis CE, Myers RH, Hunt SC, North KE. Genotype-by-sex interaction in the aetiology of type 2 diabetes mellitus: support for sex-specific quantitative trait loci in Hypertension Genetic Epidemiology Network participants. Diabetologia. 49: 2329-36. PMID 16906437 DOI: 10.1007/S00125-006-0375-4  0.323
2006 Sun M, Latourelle JC, Wooten GF, Lew MF, Klein C, Shill HA, Golbe LI, Mark MH, Racette BA, Perlmutter JS, Parsian A, Guttman M, Nicholson G, Xu G, Wilk JB, ... ... Myers RH, et al. Influence of heterozygosity for parkin mutation on onset age in familial Parkinson disease: the GenePD study. Archives of Neurology. 63: 826-32. PMID 16769863 DOI: 10.1001/Archneur.63.6.826  0.779
2006 Lloret A, Dragileva E, Teed A, Espinola J, Fossale E, Gillis T, Lopez E, Myers RH, MacDonald ME, Wheeler VC. Genetic background modifies nuclear mutant huntingtin accumulation and HD CAG repeat instability in Huntington's disease knock-in mice. Human Molecular Genetics. 15: 2015-24. PMID 16687439 DOI: 10.1093/Hmg/Ddl125  0.341
2006 Myers RH. Considerations for genomewide association studies in Parkinson disease. American Journal of Human Genetics. 78: 1081-2. PMID 16685659 DOI: 10.1086/504730  0.496
2006 Laramie JM, Wilk JB, Hunt SC, Ellison RC, Chakravarti A, Boerwinkle E, Myers RH. Evidence for a gene influencing heart rate on chromosome 5p13-14 in a meta-analysis of genome-wide scans from the NHLBI Family Blood Pressure Program. Bmc Medical Genetics. 7: 17. PMID 16509988 DOI: 10.1186/1471-2350-7-17  0.774
2006 An P, Freedman BI, Rich SS, Mandel SA, Arnett DK, Myers RH, Chen YD, Hunt SC, Rao DC. Quantitative trait loci on chromosome 8q24 for pancreatic beta-cell function and 7q11 for insulin sensitivity in obese nondiabetic white and black families: evidence from genome-wide linkage scans in the NHLBI Hypertension Genetic Epidemiology Network (HyperGEN) study. Diabetes. 55: 551-8. PMID 16443794 DOI: 10.2337/Diabetes.55.02.06.Db05-0714  0.304
2005 Karamohamed S, Latourelle JC, Racette BA, Perlmutter JS, Wooten GF, Lew M, Klein C, Shill H, Golbe LI, Mark MH, Guttman M, Nicholson G, Wilk JB, Saint-Hilaire M, DeStefano AL, ... ... Myers RH, et al. BDNF genetic variants are associated with onset age of familial Parkinson disease: GenePD Study. Neurology. 65: 1823-5. PMID 16344533 DOI: 10.1212/01.Wnl.0000187075.81589.Fd  0.809
2005 Seong IS, Ivanova E, Lee JM, Choo YS, Fossale E, Anderson M, Gusella JF, Laramie JM, Myers RH, Lesort M, MacDonald ME. HD CAG repeat implicates a dominant property of huntingtin in mitochondrial energy metabolism. Human Molecular Genetics. 14: 2871-80. PMID 16115812 DOI: 10.1093/Hmg/Ddi319  0.679
2005 Yu K, Zhang S, Borecki I, Kraja A, Xiong C, Myers R, Province M. A haplotype similarity based transmission/disequilibrium test under founder heterogeneity Annals of Human Genetics. 69: 455-467. PMID 15996173 DOI: 10.1046/J.1529-8817.2005.00168.X  0.356
2005 Karamohamed S, Golbe LI, Mark MH, Lazzarini AM, Suchowersky O, Labelle N, Guttman M, Currie LJ, Wooten GF, Stacy M, Saint-Hilaire M, Feldman RG, Liu J, Shoemaker CM, Wilk JB, ... ... Myers RH, et al. Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ-1 (T497C) genes in familial Parkinson's disease from the GenePD study. Movement Disorders : Official Journal of the Movement Disorder Society. 20: 1188-91. PMID 15966003 DOI: 10.1002/Mds.20515  0.812
2005 Friedman JH, Trieschmann ME, Myers RH, Fernandez HH. Monozygotic twins discordant for Huntington disease after 7 years. Archives of Neurology. 62: 995-7. PMID 15956172 DOI: 10.1001/Archneur.62.6.995  0.335
2004 Myers RH. Huntington's disease genetics. Neurorx : the Journal of the American Society For Experimental Neurotherapeutics. 1: 255-62. PMID 15717026 DOI: 10.1602/Neurorx.1.2.255  0.382
2004 Wilk JB, Djousse L, Arnett DK, Hunt SC, Province MA, Heiss G, Myers RH. Genome-wide linkage analyses for age at diagnosis of hypertension and early-onset hypertension in the HyperGEN study. American Journal of Hypertension. 17: 839-44. PMID 15363829 DOI: 10.1016/J.Amjhyper.2004.06.003  0.626
2004 Jiang Y, Wilk JB, Borecki I, Williamson S, DeStefano AL, Xu G, Liu J, Ellison RC, Province M, Myers RH. Common variants in the 5' region of the leptin gene are associated with body mass index in men from the National Heart, Lung, and Blood Institute Family Heart Study. American Journal of Human Genetics. 75: 220-30. PMID 15197684 DOI: 10.1086/422699  0.672
2004 Djoussé L, Knowlton B, Hayden MR, Almqvist EW, Brinkman RR, Ross CA, Margolis RL, Rosenblatt A, Durr A, Dode C, Morrison PJ, Novelletto A, Frontali M, Trent RJ, McCusker E, ... ... Myers RH, et al. Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16. Neurogenetics. 5: 109-14. PMID 15029481 DOI: 10.1007/S10048-004-0175-2  0.411
2004 Herrera VL, Didishvili T, Lopez LV, Myers RH, Ruiz-Opazo N. Genome-wide scan identifies novel QTLs for cholesterol and LDL levels in F2[Dahl RxS]-intercross rats. Circulation Research. 94: 446-52. PMID 14739155 DOI: 10.1161/01.Res.0000117770.03168.E7  0.331
2003 Karamohamed S, DeStefano AL, Wilk JB, Shoemaker CM, Golbe LI, Mark MH, Lazzarini AM, Suchowersky O, Labelle N, Guttman M, Currie LJ, Wooten GF, Stacy M, Saint-Hilaire M, Feldman RG, ... ... Myers RH, et al. A haplotype at the PARK3 locus influences onset age for Parkinson's disease: the GenePD study. Neurology. 61: 1557-61. PMID 14663042 DOI: 10.1212/01.Wnl.0000095966.99430.F4  0.717
2003 Tang W, Miller MB, Rich SS, North KE, Pankow JS, Borecki IB, Myers RH, Hopkins PN, Leppert M, Arnett DK. Linkage analysis of a composite factor for the multiple metabolic syndrome: the National Heart, Lung, and Blood Institute Family Heart Study. Diabetes. 52: 2840-7. PMID 14578304 DOI: 10.2337/Diabetes.52.11.2840  0.343
2003 Mukhopadhyay N, Finegold DN, Larson MG, Cupples LA, Myers RH, Weeks DE. A genome-wide scan for loci affecting normal adult height in the Framingham Heart Study. Human Heredity. 55: 191-201. PMID 14566097 DOI: 10.1159/000073203  0.349
2003 Gagnon DR, Glickman ME, Myers RH, Cupples LA. The analysis of survival data with a non-susceptible fraction and dual censoring mechanisms. Statistics in Medicine. 22: 3249-62. PMID 14518026 DOI: 10.1002/Sim.1568  0.361
2003 Wilk JB, DeStefano AL, Joost O, Myers RH, Cupples LA, Slater K, Atwood LD, Heard-Costa NL, Herbert A, O'Connor GT, Gottlieb DJ. Linkage and association with pulmonary function measures on chromosome 6q27 in the Framingham Heart Study. Human Molecular Genetics. 12: 2745-51. PMID 12966033 DOI: 10.1093/Hmg/Ddg311  0.659
2003 Li JL, Hayden MR, Almqvist EW, Brinkman RR, Durr A, Dodé C, Morrison PJ, Suchowersky O, Ross CA, Margolis RL, Rosenblatt A, Gómez-Tortosa E, Cabrero DM, Novelletto A, Frontali M, ... ... Myers RH, et al. A genome scan for modifiers of age at onset in Huntington disease: The HD MAPS study. American Journal of Human Genetics. 73: 682-7. PMID 12900792 DOI: 10.1086/378133  0.562
2003 Djoussé L, Knowlton B, Hayden M, Almqvist EW, Brinkman R, Ross C, Margolis R, Rosenblatt A, Durr A, Dode C, Morrison PJ, Novelletto A, Frontali M, Trent RJ, McCusker E, ... ... Myers RH, et al. Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington disease. American Journal of Medical Genetics. Part A. 119: 279-82. PMID 12784292 DOI: 10.1002/Ajmg.A.20190  0.366
2003 Wu X, Cooper RS, Boerwinkle E, Turner ST, Hunt S, Myers R, Olshen RA, Curb D, Zhu X, Kan D, Luke A. Combined analysis of genomewide scans for adult height: results from the NHLBI Family Blood Pressure Program. European Journal of Human Genetics : Ejhg. 11: 271-4. PMID 12673281 DOI: 10.1038/Sj.Ejhg.5200952  0.326
2003 Wilk JB, DeStefano AL, Arnett DK, Rich SS, Djousse L, Crapo RO, Leppert MF, Province MA, Cupples LA, Gottlieb DJ, Myers RH. A genome-wide scan of pulmonary function measures in the National Heart, Lung, and Blood Institute Family Heart Study. American Journal of Respiratory and Critical Care Medicine. 167: 1528-33. PMID 12637344 DOI: 10.1164/Rccm.200207-755Oc  0.637
2003 DeStefano AL, Gates GA, Heard-Costa N, Myers RH, Baldwin CT. Genomewide linkage analysis to presbycusis in the Framingham Heart Study. Archives of Otolaryngology--Head & Neck Surgery. 129: 285-9. PMID 12622536 DOI: 10.1001/Archotol.129.3.285  0.373
2002 Van Laer L, DeStefano AL, Myers RH, Flothmann K, Thys S, Fransen E, Gates GA, Van Camp G, Baldwin CT. Is DFNA5 a susceptibility gene for age-related hearing impairment? European Journal of Human Genetics : Ejhg. 10: 883-6. PMID 12461698 DOI: 10.1038/Sj.Ejhg.5200878  0.346
2002 Djoussé L, Knowlton B, Cupples LA, Marder K, Shoulson I, Myers RH. Weight loss in early stage of Huntington's disease. Neurology. 59: 1325-30. PMID 12427878 DOI: 10.1212/01.Wnl.0000031791.10922.Cf  0.343
2002 Karasik D, Myers RH, Hannan MT, Gagnon D, McLean RR, Cupples LA, Kiel DP. Mapping of quantitative ultrasound of the calcaneus bone to chromosome 1 by genome-wide linkage analysis. Osteoporosis International : a Journal Established as Result of Cooperation Between the European Foundation For Osteoporosis and the National Osteoporosis Foundation of the Usa. 13: 796-802. PMID 12378368 DOI: 10.1007/S001980200110  0.354
2002 Coon H, Eckfeldt JH, Leppert MF, Myers RH, Arnett DK, Heiss G, Province MA, Hunt SC. A genome-wide screen reveals evidence for a locus on chromosome 11 influencing variation in LDL cholesterol in the NHLBI Family Heart Study. Human Genetics. 111: 263-9. PMID 12215839 DOI: 10.1007/S00439-002-0773-8  0.334
2002 Karasik D, Myers RH, Cupples LA, Hannan MT, Gagnon DR, Herbert A, Kiel DP. Genome screen for quantitative trait loci contributing to normal variation in bone mineral density: the Framingham Study. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 17: 1718-27. PMID 12211443 DOI: 10.1359/Jbmr.2002.17.9.1718  0.326
2002 Wilk JB, Myers RH, Zhang Y, Lewis CE, Atwood L, Hopkins PN, Ellison RC. Evidence for a gene influencing heart rate on chromosome 4 among hypertensives. Human Genetics. 111: 207-13. PMID 12189495 DOI: 10.1007/S00439-002-0780-9  0.65
2002 Maher NE, Currie LJ, Lazzarini AM, Wilk JB, Taylor CA, Saint-Hilaire MH, Feldman RG, Golbe LI, Wooten GF, Myers RH. Segregation analysis of Parkinson disease revealing evidence for a major causative gene. American Journal of Medical Genetics. 109: 191-7. PMID 11977177 DOI: 10.1002/Ajmg.10335  0.711
2002 DeStefano AL, Lew MF, Golbe LI, Mark MH, Lazzarini AM, Guttman M, Montgomery E, Waters CH, Singer C, Watts RL, Currie LJ, Wooten GF, Maher NE, Wilk JB, Sullivan KM, ... ... Myers RH, et al. PARK3 influences age at onset in Parkinson disease: a genome scan in the GenePD study. American Journal of Human Genetics. 70: 1089-95. PMID 11920285 DOI: 10.1086/339814  0.711
2002 Joost O, Wilk JB, Cupples LA, Harmon M, Shearman AM, Baldwin CT, O'Connor GT, Myers RH, Gottlieb DJ. Genetic loci influencing lung function: a genome-wide scan in the Framingham Study. American Journal of Respiratory and Critical Care Medicine. 165: 795-9. PMID 11897646 DOI: 10.1164/Ajrccm.165.6.2102057  0.639
2002 Meigs JB, Panhuysen CI, Myers RH, Wilson PW, Cupples LA. A genome-wide scan for loci linked to plasma levels of glucose and HbA(1c) in a community-based sample of Caucasian pedigrees: The Framingham Offspring Study. Diabetes. 51: 833-40. PMID 11872688 DOI: 10.2337/Diabetes.51.3.833  0.317
2002 Maher NE, Golbe LI, Lazzarini AM, Mark MH, Currie LJ, Wooten GF, Saint-Hilaire M, Wilk JB, Volcjak J, Maher JE, Feldman RG, Guttman M, Lew M, Waters CH, Schuman S, ... ... Myers RH, et al. Epidemiologic study of 203 sibling pairs with Parkinson's disease: the GenePD study. Neurology. 58: 79-84. PMID 11781409 DOI: 10.1212/Wnl.58.1.79  0.693
2002 Feitosa MF, Borecki IB, Rich SS, Arnett DK, Sholinsky P, Myers RH, Leppert M, Province MA. Quantitative-trait loci influencing body-mass index reside on chromosomes 7 and 13: the National Heart, Lung, and Blood Institute Family Heart Study. American Journal of Human Genetics. 70: 72-82. PMID 11713718 DOI: 10.1086/338144  0.366
2001 Heard-Costa NL, Demissie S, DeStefano AL, Knowlton BA, Maher NE, Myers RH, Volcjak JS, Wilk JB, Cupples LA. Influence of marker heterozygosity and genetic heterogeneity on fine mapping. Genetic Epidemiology. 21: S467-72. PMID 11793720 DOI: 10.1002/Gepi.2001.21.S1.S467  0.632
2001 Wilk JB, Volcjak JS, Myers RH, Maher NE, Knowlton BA, Heard-Costa NL, Demissie S, Cupples LA, DeStefano AL. Family-based association tests for qualitative and quantitative traits using single-nucleotide polymorphism and microsatellite data. Genetic Epidemiology. 21: S364-9. PMID 11793700 DOI: 10.1002/Gepi.2001.21.S1.S364  0.667
2001 Coon H, Leppert MF, Eckfeldt JH, Oberman A, Myers RH, Peacock JM, Province MA, Hopkins PN, Heiss G. Genome-wide linkage analysis of lipids in the Hypertension Genetic Epidemiology Network (HyperGEN) Blood Pressure Study. Arteriosclerosis, Thrombosis, and Vascular Biology. 21: 1969-76. PMID 11742872 DOI: 10.1161/Hq1201.100228  0.32
2001 Gottlieb DJ, Wilk JB, Harmon M, Evans JC, Joost O, Levy D, O'Connor GT, Myers RH. Heritability of longitudinal change in lung function. The Framingham study. American Journal of Respiratory and Critical Care Medicine. 164: 1655-9. PMID 11719305 DOI: 10.1164/Ajrccm.164.9.2010122  0.606
2001 Peacock JM, Arnett DK, Atwood LD, Myers RH, Coon H, Rich SS, Province MA, Heiss G. Genome scan for quantitative trait loci linked to high-density lipoprotein cholesterol: The NHLBI Family Heart Study. Arteriosclerosis, Thrombosis, and Vascular Biology. 21: 1823-8. PMID 11701472 DOI: 10.1161/Hq1101.097804  0.333
2001 DeStefano AL, Golbe LI, Mark MH, Lazzarini AM, Maher NE, Saint-Hilaire M, Feldman RG, Guttman M, Watts RL, Suchowersky O, Lafontaine AL, Labelle N, Lew MF, Waters CH, Growdon JH, ... ... Myers RH, et al. Genome-wide scan for Parkinson's disease: the GenePD Study. Neurology. 57: 1124-6. PMID 11571351 DOI: 10.1212/Wnl.57.6.1124  0.428
2001 Nance MA, Myers RH. Juvenile onset Huntington's disease--clinical and research perspectives. Mental Retardation and Developmental Disabilities Research Reviews. 7: 153-7. PMID 11553930 DOI: 10.1002/Mrdd.1022  0.36
2001 Glorioso N, Filigheddu F, Troffa C, Soro A, Parpaglia PP, Tsikoudakis A, Myers RH, Herrera VL, Ruiz-Opazo N. Interaction of alpha(1)-Na,K-ATPase and Na,K,2Cl-cotransporter genes in human essential hypertension. Hypertension. 38: 204-9. PMID 11509477 DOI: 10.1161/01.Hyp.38.2.204  0.338
2001 Hunt SC, Kronenberg F, Eckfeldt JH, Hopkins PN, Myers RH, Heiss G. Association of plasma bilirubin with coronary heart disease and segregation of bilirubin as a major gene trait: the NHLBI family heart study. Atherosclerosis. 154: 747-54. PMID 11257278 DOI: 10.1016/S0021-9150(00)00420-2  0.334
2001 Gómez-Tortosa E, MacDonald ME, Friend JC, Taylor SA, Weiler LJ, Cupples LA, Srinidhi J, Gusella JF, Bird ED, Vonsattel JP, Myers RH. Quantitative neuropathological changes in presymptomatic Huntington's disease. Annals of Neurology. 49: 29-34. PMID 11198293 DOI: 10.1002/1531-8249(200101)49:1<29::Aid-Ana7>3.0.Co;2-B  0.373
2000 Zee RY, Myers RH, Hannan MT, Wilson PW, Ordovas JM, Schaefer EJ, Lindpaintner K, Kiel DP. Absence of linkage for bone mineral density to chromosome 12q12-14 in the region of the vitamin D receptor gene. Calcified Tissue International. 67: 434-9. PMID 11289690 DOI: 10.1007/S002230001175  0.33
2000 Levy D, DeStefano AL, Larson MG, O'Donnell CJ, Lifton RP, Gavras H, Cupples LA, Myers RH. Evidence for a gene influencing blood pressure on chromosome 17. Genome scan linkage results for longitudinal blood pressure phenotypes in subjects from the framingham heart study. Hypertension. 36: 477-83. PMID 11040222 DOI: 10.1161/01.Hyp.36.4.477  0.351
2000 Coon H, Myers RH, Borecki IB, Arnett DK, Hunt SC, Province MA, Djousse L, Leppert MF. Replication of linkage of familial combined hyperlipidemia to chromosome 1q with additional heterogeneous effect of apolipoprotein A-I/C-III/A-IV locus. The NHLBI Family Heart Study. Arteriosclerosis, Thrombosis, and Vascular Biology. 20: 2275-80. PMID 11031215 DOI: 10.1161/01.Atv.20.10.2275  0.358
2000 Salomaa V, Pankow J, Heiss G, Cakir B, Eckfeldt JH, Ellison RC, Myers RH, Hiller KM, Brantley KR, Morris TL, Weston BW. Genetic background of Lewis negative blood group phenotype and its association with atherosclerotic disease in the NHLBI family heart study. Journal of Internal Medicine. 247: 689-98. PMID 10886491 DOI: 10.1046/J.1365-2796.2000.00682.X  0.335
2000 Wilk JB, Djousse L, Arnett DK, Rich SS, Province MA, Hunt SC, Crapo RO, Higgins M, Myers RH. Evidence for major genes influencing pulmonary function in the NHLBI family heart study. Genetic Epidemiology. 19: 81-94. PMID 10861898 DOI: 10.1002/1098-2272(200007)19:1<81::Aid-Gepi6>3.0.Co;2-8  0.643
2000 Shearman AM, Ordovas JM, Cupples LA, Schaefer EJ, Harmon MD, Shao Y, Keen JD, DeStefano AL, Joost O, Wilson PW, Housman DE, Myers RH. Evidence for a gene influencing the TG/HDL-C ratio on chromosome 7q32.3-qter: a genome-wide scan in the Framingham study. Human Molecular Genetics. 9: 1315-20. PMID 10814713 DOI: 10.1093/Hmg/9.9.1315  0.307
2000 Wilk JB, Djousse L, Borecki I, Atwood LD, Hunt SC, Rich SS, Eckfeldt JH, Arnett DK, Rao DC, Myers RH. Segregation analysis of serum uric acid in the NHLBI Family Heart Study. Human Genetics. 106: 355-9. PMID 10798367 DOI: 10.1007/S004390051050  0.628
1999 Coon H, Leppert MF, Kronenberg F, Province MA, Myers RH, Arnett DK, Eckfeldt JH, Heiss G, Williams RR, Hunt SC. Evidence for a major gene accounting for mild elevation in LDL cholesterol: the NHLBI Family Heart Study. Annals of Human Genetics. 63: 401-12. PMID 10735582 DOI: 10.1046/J.1469-1809.1999.6350401.X  0.316
1999 Wilk JB, Premkumar S, Nicolaou M, Myers RH, Maher NE, Harmon MD, Farrer LA, DeStefano AL, Cupples LA, Couropmitree NN. Stratification techniques to explore genotype environment interactions. Genetic Epidemiology. 17: S761-6. PMID 10597527 DOI: 10.1002/Gepi.13701707125  0.65
1999 Taylor CA, Saint-Hilaire MH, Cupples LA, Thomas CA, Burchard AE, Feldman RG, Myers RH. Environmental, medical, and family history risk factors for Parkinson's disease: a New England-based case control study. American Journal of Medical Genetics. 88: 742-9. PMID 10581500 DOI: 10.1002/(Sici)1096-8628(19991215)88:6<742::Aid-Ajmg29>3.0.Co;2-#  0.428
1999 MacDonald ME, Vonsattel JP, Shrinidhi J, Couropmitree NN, Cupples LA, Bird ED, Gusella JF, Myers RH. Evidence for the GluR6 gene associated with younger onset age of Huntington's disease. Neurology. 53: 1330-2. PMID 10522893 DOI: 10.1212/Wnl.53.6.1330  0.42
1999 Joost O, Taylor CA, Thomas CA, Cupples LA, Saint-Hilaire MH, Feldman RG, Baldwin CT, Myers RH. Absence of effect of seven functional mutations in the CYP2D6 gene in Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 14: 590-5. PMID 10435495 DOI: 10.1002/1531-8257(199907)14:4<590::AID-MDS1007>3.0.CO;2-2  0.33
1999 Karluk D, Myers RH, DiFiglia M, Gusella JF, MacDonald ME, Penney JB, Young AB, Hobbs W, Lenzi S, Srinidhi S, Hedley-Whyte ET, Vonsattel J. NONAGENARIANS WITH HUNTINGTON DISEASE (HD) HAVE LOW CAG REPEATS Journal of Neuropathology and Experimental Neurology. 58: 549. DOI: 10.1097/00005072-199905000-00170  0.31
1998 Arnett DK, Borecki IB, Ludwig EH, Pankow JS, Myers R, Evans G, Folsom AR, Heiss G, Higgins M. Angiotensinogen and angiotensin converting enzyme genotypes and carotid atherosclerosis: the atherosclerosis risk in communities and the NHLBI family heart studies. Atherosclerosis. 138: 111-6. PMID 9678776 DOI: 10.1016/S0021-9150(98)00009-4  0.329
1998 Pocovi M, Cenarro A, Civeira F, Torralba MA, Perez-Calvo JI, Mozas P, Giraldo P, Giralt M, Myers RH, Cupples LA, Ordovas JM. Beta-glucocerebrosidase gene locus as a link for Gaucher's disease and familial hypo-alpha-lipoproteinaemia. Lancet. 351: 1919-23. PMID 9654259 DOI: 10.1016/S0140-6736(97)09490-7  0.311
1998 Givelber RJ, Couropmitree NN, Gottlieb DJ, Evans JC, Levy D, Myers RH, O'Connor GT. Segregation analysis of pulmonary function among families in the Framingham Study. American Journal of Respiratory and Critical Care Medicine. 157: 1445-51. PMID 9603122 DOI: 10.1164/Ajrccm.157.5.9704021  0.312
1998 Jenkins BG, Rosas HD, Chen YC, Makabe T, Myers R, MacDonald M, Rosen BR, Beal MF, Koroshetz WJ. 1H NMR spectroscopy studies of Huntington's disease: correlations with CAG repeat numbers. Neurology. 50: 1357-65. PMID 9595987 DOI: 10.1212/Wnl.50.5.1357  0.335
1997 DeStefano AL, Cupples LA, Myers RH, Farrer LA. Detecting linkage for a complex disease using simulated extended pedigrees. Genetic Epidemiology. 14: 981-6. PMID 9433611 DOI: 10.1002/(Sici)1098-2272(1997)14:6<981::Aid-Gepi70>3.0.Co;2-G  0.351
1997 Aaltonen J, Horelli-Kuitunen N, Fan J, Björses P, Perheentupa J, Myers R, Palotie A, Peltonen L. High-Resolution Physical and Transcriptional Mapping of the Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Locus on Chromosome 21q22.3 by FISH Genome Research. 7: 820-829. PMID 9267805 DOI: 10.1101/Gr.7.8.820  0.334
1997 McNeil SM, Novelletto A, Srinidhi J, Barnes G, Kornbluth I, Altherr MR, Wasmuth JJ, Gusella JF, MacDonald ME, Myers RH. Reduced penetrance of the Huntington's disease mutation. Human Molecular Genetics. 6: 775-9. PMID 9158152 DOI: 10.1093/Hmg/6.5.775  0.341
1997 Penney JB, Vonsattel JP, MacDonald ME, Gusella JF, Myers RH. CAG repeat number governs the development rate of pathology in Huntington's disease. Annals of Neurology. 41: 689-92. PMID 9153534 DOI: 10.1002/Ana.410410521  0.356
1996 Gusella JF, McNeil S, Persichetti F, Srinidhi J, Novelletto A, Bird E, Faber P, Vonsattel JP, Myers RH, MacDonald ME. Huntington's disease. Cold Spring Harbor Symposia On Quantitative Biology. 61: 615-26. PMID 9246488 DOI: 10.1055/S-2008-1063867  0.305
1995 Leeflang EP, Zhang L, Tavaré S, Hubert R, Srinidhi J, MacDonald ME, Myers RH, de Young M, Wexler NS, Gusella JF. Single sperm analysis of the trinucleotide repeats in the Huntington's disease gene: quantification of the mutation frequency spectrum. Human Molecular Genetics. 4: 1519-26. PMID 8541834 DOI: 10.1093/Hmg/4.9.1519  0.318
1995 Wilson PW, Myers RH, Larson MG, Ordovas JM, Wolf PA, Schaefer EJ. 750-5 Apolipoprotein E Alleles, Dyslipidemia, and Coronary Heart Disease: The Framingham Offspring Study Journal of the American College of Cardiology. 25: 196A. DOI: 10.1016/0735-1097(95)92270-F  0.306
1995 Levy D, Lindpaintner K, Larson MG, Ramachandran VS, Myers RH, Pfeffer MA, Ordovas JM, Schaefer EJ, Wilson PW. 729-4 Left Ventricular Hypertrophy and the Deletion-Insertion Polymorphism of the Angiotensin Converting Enzyme Gene Journal of the American College of Cardiology. 25: 136A. DOI: 10.1016/0735-1097(95)92019-2  0.335
1995 Ramachandran VS, Levy D, Larson MG, Ordovas JM, Schaefer EJ, Myers RH, Lindpaintner K, Wilson PW. 901-81 Association of a Molecular Variant of the Angiotensinogen Gene and Hypertension Journal of the American College of Cardiology. 25: 24A. DOI: 10.1016/0735-1097(95)91558-F  0.369
1994 Persichetti F, Srinidhi J, Kanaley L, Ge P, Myers RH, D'Arrigo K, Barnes GT, MacDonald ME, Vonsattel JP, Gusella JF. Huntington's disease CAG trinucleotide repeats in pathologically confirmed post-mortem brains. Neurobiology of Disease. 1: 159-66. PMID 9173995 DOI: 10.1006/Nbdi.1994.0019  0.368
1994 Lazzarini AM, Myers RH, Zimmerman TR, Mark MH, Golbe LI, Sage JI, Johnson WG, Duvoisin RC. A clinical genetic study of Parkinson's disease: evidence for dominant transmission. Neurology. 44: 499-506. PMID 8145922 DOI: 10.1212/Wnl.44.3_Part_1.499  0.429
1993 MacDonald ME, Ambrose CM, Duyao MP, Myers RH, Lin C, Srinidhi L, Barnes G, Taylor SA, James M, Groot N, MacFarlane H, Jenkins B, Anderson MA, Wexler NS, Gusella JF, et al. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes Cell. 72: 971-983. PMID 8458085 DOI: 10.1016/0092-8674(93)90585-E  0.407
1993 Duyao M, Ambrose C, Myers R, Novelletto A, Persichetti F, Frontali M, Folstein S, Ross C, Franz M, Abbott M, Gray J, Conneally P, Young A, Penney J, Hollingsworth Z, et al. Trinucleotide repeat length instability and age of onset in Huntington's disease Nature Genetics. 4: 387-392. PMID 8401587 DOI: 10.1038/Ng0893-387  0.371
1992 Ogawa T, Matson WR, Beal MF, Myers RH, Bird ED, Milbury P, Saso S. Kynurenine pathway abnormalities in Parkinson's disease. Neurology. 42: 1702-6. PMID 1513457 DOI: 10.1212/Wnl.42.9.1702  0.387
1992 Diamond R, White RF, Myers RH, Mastromauro C, Koroshetz WJ, Butters N, Rothstein DM, Moss MB, Vasterling J. Evidence of presymptomatic cognitive decline in Huntington's disease. Journal of Clinical and Experimental Neuropsychology. 14: 961-75. PMID 1452640 DOI: 10.1080/01688639208402547  0.323
1992 MacDonald ME, Novelletto A, Lin C, Tagle D, Barnes G, Bates G, Taylor S, Allitto B, Altherr M, Myers R. The Huntington's disease candidate region exhibits many different haplotypes. Nature Genetics. 1: 99-103. PMID 1302016 DOI: 10.1038/Ng0592-99  0.387
1990 St George-Hyslop PH, Haines JL, Farrer LA, Polinsky R, Van Broeckhoven C, Goate A, McLachlan DR, Orr H, Bruni AC, Sorbi S, Rainero I, Foncin JF, Pollen D, Cantu JM, Tupler R, ... ... Myers RH, et al. Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder. Nature. 347: 194-7. PMID 2395471 DOI: 10.1038/347194A0  0.383
1990 Farrer LA, Myers RH, Cupples LA, St George-Hyslop PH, Bird TD, Rossor MN, Mullan MJ, Polinsky R, Nee L, Heston L. Transmission and age-at-onset patterns in familial Alzheimer's disease: evidence for heterogeneity. Neurology. 40: 395-403. PMID 2314579 DOI: 10.1097/00002093-199100510-00015  0.326
1989 Farrer LA, O'Sullivan DM, Cupples LA, Growdon JH, Myers RH. Assessment of genetic risk for Alzheimer's disease among first-degree relatives. Annals of Neurology. 25: 485-93. PMID 2774490 DOI: 10.1002/Ana.410250511  0.333
1989 St George-Hyslop PH, Tanzi RE, Haines JL, Polinsky RJ, Farrer L, Myers RH, Gusella JF. Molecular genetics of familial Alzheimer's disease. European Neurology. 29: 25-7. PMID 2693103 DOI: 10.1159/000116477  0.385
1989 St George-Hyslop PH, Myers RH, Haines JL, Farrer LA, Tanzi RE, Abe K, James MF, Conneally PM, Polinsky RJ, Gusella JF. Familial Alzheimer's disease: progress and problems. Neurobiology of Aging. 10: 417-25. PMID 2682321 DOI: 10.1016/0197-4580(89)90082-1  0.303
1989 St George-Hyslop PH, Haines JL, Polinsky RJ, Tanzi RE, Farrer L, Myers RH, Gusella JF. Molecular genetics of familial Alzheimer's disease. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 16: 465-7. PMID 2680005 DOI: 10.1017/S0317167100029772  0.351
1989 Conneally PM, Haines JL, Tanzi RE, Wexler NS, Penchaszadeh GK, Harper PS, Folstein SE, Cassiman JJ, Myers RH, Young AB. Huntington disease: no evidence for locus heterogeneity. Genomics. 5: 304-8. PMID 2571579 DOI: 10.1016/0888-7543(89)90062-1  0.333
1989 Sax DS, Bird ED, Gusella JF, Myers RH. Phenotypic variation in 2 Huntington's disease families with linkage to chromosome 4. Neurology. 39: 1332-6. PMID 2529452 DOI: 10.1212/Wnl.39.10.1332  0.407
1989 Mastromauro CA, Meissen GJ, Cupples LA, Kiely DK, Berkman B, Myers RH. Estimation of fertility and fitness in Huntington disease in New England. American Journal of Medical Genetics. 33: 248-54. PMID 2527461 DOI: 10.1002/Ajmg.1320330222  0.303
1989 Cupples LA, Terrin NC, Myers RH, D'Agostino RB. Using survival methods to estimate age-at-onset distributions for genetic diseases with an application to Huntington disease. Genetic Epidemiology. 6: 361-71. PMID 2524419 DOI: 10.1002/Gepi.1370060206  0.321
1988 Myers RH, Vonsattel JP, Stevens TJ, Cupples LA, Richardson EP, Martin JB, Bird ED. Clinical and neuropathologic assessment of severity in Huntington's disease. Neurology. 38: 341-7. PMID 2964565 DOI: 10.1212/Wnl.38.3.341  0.35
1988 Farrer LA, Myers RH, Cupples LA, Conneally PM. Considerations in using linkage analysis as a presymptomatic test for Huntington's disease. Journal of Medical Genetics. 25: 577-88. PMID 2903248 DOI: 10.1136/Jmg.25.9.577  0.323
1988 Meissen GJ, Myers RH, Mastromauro CA, Koroshetz WJ, Klinger KW, Farrer LA, Watkins PA, Gusella JF, Bird ED, Martin JB. Predictive testing for Huntington's disease with use of a linked DNA marker. The New England Journal of Medicine. 318: 535-42. PMID 2893260 DOI: 10.1056/Nejm198803033180903  0.341
1987 St George-Hyslop PH, Tanzi RE, Polinsky RJ, Neve RL, Pollen D, Drachman D, Growdon J, Cupples LA, Nee L, Myers RH. Absence of duplication of chromosome 21 genes in familial and sporadic Alzheimer's disease. Science (New York, N.Y.). 238: 664-6. PMID 2890206 DOI: 10.1126/Science.2890206  0.322
1987 St George-Hyslop PH, Tanzi RE, Polinsky RJ, Haines JL, Nee L, Watkins PC, Myers RH, Feldman RG, Pollen D, Drachman D. The genetic defect causing familial Alzheimer's disease maps on chromosome 21. Science (New York, N.Y.). 235: 885-90. PMID 2880399 DOI: 10.1126/Science.2880399  0.361
1985 Myers RH, Sax DS, Schoenfeld M, Bird ED, Wolf PA, Vonsattel JP, White RF, Martin JB. Late onset of Huntington's disease. Journal of Neurology, Neurosurgery, and Psychiatry. 48: 530-4. PMID 3159849 DOI: 10.1136/Jnnp.48.6.530  0.334
1983 Sudarsky L, Myers RH, Walshe TM. Huntington's disease in monozygotic twins reared apart. Journal of Medical Genetics. 20: 408-11. PMID 6228662 DOI: 10.1136/Jmg.20.6.408  0.346
1982 Sinex FM, Myers RH. Alzheimer's disease, Down's syndrome, and aging: the genetic approach. Annals of the New York Academy of Sciences. 396: 3-13. PMID 6217775 DOI: 10.1111/J.1749-6632.1982.Tb26839.X  0.305
Low-probability matches (unlikely to be authored by this person)
1994 Wilson PW, Myers RH, Larson MG, Ordovas JM, Wolf PA, Schaefer EJ. Apolipoprotein E alleles, dyslipidemia, and coronary heart disease. The Framingham Offspring Study. Jama. 272: 1666-71. PMID 7966894 DOI: 10.1001/Jama.1994.03520210050031  0.3
2014 Bharadwaj R, Peter CJ, Jiang Y, Roussos P, Vogel-Ciernia A, Shen EY, Mitchell AC, Mao W, Whittle C, Dincer A, Jakovcevski M, Pothula V, Rasmussen TP, Giakoumaki SG, Bitsios P, ... ... Myers RH, et al. Conserved higher-order chromatin regulates NMDA receptor gene expression and cognition. Neuron. 84: 997-1008. PMID 25467983 DOI: 10.1016/J.Neuron.2014.10.032  0.299
2004 Avery CL, Freedman BI, Heiss G, Kraja A, Rice T, Arnett D, Miller MB, Pankow JS, Lewis CE, Myers RH, Hunt SC, Almasy L, North KE. Linkage analysis of diabetes status among hypertensive families: the Hypertension Genetic Epidemiology Network study. Diabetes. 53: 3307-12. PMID 15561964 DOI: 10.2337/Diabetes.53.12.3307  0.299
2005 Kraja AT, Hunt SC, Pankow JS, Myers RH, Heiss G, Lewis CE, Rao DC, Province MA. Quantitative trait loci for metabolic syndrome in the Hypertension Genetic Epidemiology Network study. Obesity Research. 13: 1885-90. PMID 16339118 DOI: 10.1038/Oby.2005.231  0.299
1994 Gaston S, Myers R, White R, Tanzi R, Feldman R. Clinical phenotype of chromosome 14q24 associated FAD in the Italian-American (Feldman FAD Family) pedigree Neurobiology of Aging. 15: S9. DOI: 10.1016/0197-4580(94)92487-2  0.299
1993 MacDonald ME, Barnes G, Srinidhi J, Duyao MP, Ambrose CM, Myers RH, Gray J, Conneally PM, Young A, Penney J. Gametic but not somatic instability of CAG repeat length in Huntington's disease. Journal of Medical Genetics. 30: 982-6. PMID 8133508 DOI: 10.1136/Jmg.30.12.982  0.299
1999 Ellison RC, Zhang Y, Myers RH, Swanson JL, Higgins M, Eckfeldt J. Lewis blood group phenotype as an independent risk factor for coronary heart disease (the NHLBI Family Heart Study). The American Journal of Cardiology. 83: 345-8. PMID 10072221 DOI: 10.1016/S0002-9149(98)00866-2  0.296
2004 Djoussé L, Pankow JS, Arnett DK, Eckfeldt JH, Myers RH, Ellison RC. Apolipoprotein E polymorphism modifies the alcohol-HDL association observed in the National Heart, Lung, and Blood Institute Family Heart Study. The American Journal of Clinical Nutrition. 80: 1639-44. PMID 15585780 DOI: 10.1093/Ajcn/80.6.1639  0.294
1984 Schoenfeld M, Berkman B, Myers RH, Clark E. Attitudes toward marriage and childbearing of individuals at risk for Huntington's disease. Social Work in Health Care. 9: 73-81. PMID 6237443 DOI: 10.1300/J010V09N04_07  0.294
1996 Lindpaintner K, Lee M, Larson MG, Rao VS, Pfeffer MA, Ordovas JM, Schaefer EJ, Wilson AF, Wilson PW, Vasan RS, Myers RH, Levy D. Absence of association or genetic linkage between the angiotensin-converting-enzyme gene and left ventricular mass. The New England Journal of Medicine. 334: 1023-8. PMID 8598840 DOI: 10.1056/Nejm199604183341604  0.294
1992 Brand FN, Kiely DK, Kannel WB, Myers RH. Family patterns of coronary heart disease mortality: the Framingham Longevity Study. Journal of Clinical Epidemiology. 45: 169-74. PMID 1573433 DOI: 10.1016/0895-4356(92)90009-C  0.293
2014 McCusker EA, Myers RH. Feasibility of Huntington disease trials in the disease prodrome. Neurology. 82: 824-5. PMID 24510495 DOI: 10.1212/Wnl.0000000000000197  0.291
1991 Myers RH, Vonsattel JP, Paskevich PA, Kiely DK, Stevens TJ, Cupples LA, Richardson EP, Bird ED. Decreased neuronal and increased oligodendroglial densities in Huntington's disease caudate nucleus. Journal of Neuropathology and Experimental Neurology. 50: 729-42. PMID 1836225 DOI: 10.1097/00005072-199111000-00005  0.291
1998 Felson DT, Couropmitree NN, Chaisson CE, Hannan MT, Zhang Y, McAlindon TE, LaValley M, Levy D, Myers RH. Evidence for a Mendelian gene in a segregation analysis of generalized radiographic osteoarthritis: the Framingham Study. Arthritis and Rheumatism. 41: 1064-71. PMID 9627016 DOI: 10.1002/1529-0131(199806)41:6<1064::Aid-Art13>3.0.Co;2-K  0.291
1999 Gates GA, Couropmitree NN, Myers RH. Genetic associations in age-related hearing thresholds. Archives of Otolaryngology--Head & Neck Surgery. 125: 654-9. PMID 10367922 DOI: 10.1001/Archotol.125.6.654  0.29
2000 Marder K, Zhao H, Myers RH, Cudkowicz M, Kayson E, Kieburtz K, Orme C, Paulsen J, Penney JB, Siemers E, Shoulson I. Rate of functional decline in Huntington's disease. Huntington Study Group. Neurology. 54: 452-8. PMID 10668713 DOI: 10.1212/Wnl.54.2.452  0.29
1997 Kiel DP, Myers RH, Cupples LA, Kong XF, Zhu XH, Ordovas J, Schaefer EJ, Felson DT, Rush D, Wilson PW, Eisman JA, Holick MF. The BsmI vitamin D receptor restriction fragment length polymorphism (bb) influences the effect of calcium intake on bone mineral density. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 12: 1049-57. PMID 9200004 DOI: 10.1359/Jbmr.1997.12.7.1049  0.289
2015 Biglan KM, Shoulson I, Kieburtz K, Oakes D, Kayson E, Shinaman MA, Zhao H, Romer M, Young A, Hersch S, Penney J, Marder K, Paulsen J, Quaid K, ... ... Myers R, et al. Clinical-Genetic Associations in the Prospective Huntington at Risk Observational Study (PHAROS): Implications for Clinical Trials. Jama Neurology. 1-9. PMID 26569098 DOI: 10.1001/Jamaneurol.2015.2736  0.288
1999 Feng D, Lindpaintner K, Larson MG, Rao VS, O'Donnell CJ, Lipinska I, Schmitz C, Sutherland PA, Silbershatz H, D'Agostino RB, Muller JE, Myers RH, Levy D, Tofler GH. Increased platelet aggregability associated with platelet GPIIIa PlA2 polymorphism: the Framingham Offspring Study. Arteriosclerosis, Thrombosis, and Vascular Biology. 19: 1142-7. PMID 10195947 DOI: 10.1161/01.Atv.19.4.1142  0.288
1996 Pocovi M, Cenarro A, Civeira F, Myers RH, Casao E, Esteban M, Ordovas JM. Incomplete dominance of type III hyperlipoproteinemia is associated with the rare apolipoprotein E2 (Arg136-->Ser) variant in multigenerational pedigree studies. Atherosclerosis. 122: 33-46. PMID 8724110 DOI: 10.1016/0021-9150(95)06745-0  0.288
1985 Vonsattel JP, Myers RH, Stevens TJ, Ferrante RJ, Bird ED, Richardson EP. Neuropathological classification of Huntington's disease. Journal of Neuropathology and Experimental Neurology. 44: 559-77. PMID 2932539 DOI: 10.1097/00005072-198511000-00003  0.288
2003 Wheelock VL, Tempkin T, Marder K, Nance M, Myers RH, Zhao H, Kayson E, Orme C, Shoulson I. Predictors of nursing home placement in Huntington disease. Neurology. 60: 998-1001. PMID 12654967 DOI: 10.1212/01.Wnl.0000052992.58107.67  0.286
1984 Schoenfeld M, Myers RH, Berkman B, Clark E. Potential impact of a predictive test on the gene frequency of Huntington disease. American Journal of Medical Genetics. 18: 423-9. PMID 6236692 DOI: 10.1002/Ajmg.1320180311  0.284
2003 Gasser T, Bressman S, Dürr A, Higgins J, Klockgether T, Myers RH. State of the art review: molecular diagnosis of inherited movement disorders. Movement Disorders Society task force on molecular diagnosis. Movement Disorders : Official Journal of the Movement Disorder Society. 18: 3-18. PMID 12518296 DOI: 10.1002/Mds.10338  0.282
1984 Schoenfeld M, Myers RH, Cupples LA, Berkman B, Sax DS, Clark E. Increased rate of suicide among patients with Huntington's disease. Journal of Neurology, Neurosurgery, and Psychiatry. 47: 1283-7. PMID 6239910 DOI: 10.1136/Jnnp.47.12.1283  0.282
1989 Schildkraut JM, Myers RH, Cupples LA, Kiely DK, Kannel WB. Coronary risk associated with age and sex of parental heart disease in the Framingham Study. The American Journal of Cardiology. 64: 555-9. PMID 2782245 DOI: 10.1016/0002-9149(89)90477-3  0.277
1998 O'Donnell CJ, Lindpaintner K, Larson MG, Rao VS, Ordovas JM, Schaefer EJ, Myers RH, Levy D. Evidence for association and genetic linkage of the angiotensin-converting enzyme locus with hypertension and blood pressure in men but not women in the Framingham Heart Study. Circulation. 97: 1766-72. PMID 9603529 DOI: 10.1161/01.Cir.97.18.1766  0.276
1996 Sax DS, Powsner R, Kim A, Tilak S, Bhatia R, Cupples LA, Myers RH. Evidence of cortical metabolic dysfunction in early Huntington's disease by single-photon-emission computed tomography. Movement Disorders : Official Journal of the Movement Disorder Society. 11: 671-7. PMID 8914093 DOI: 10.1002/Mds.870110612  0.276
1997 G. Vonsattel J-, Zhao Y, Lenzi S, Gómez-Isla T, Hyman BT, Myers R, DiFielia M, Gusella J, MacDonald M, Ma MJ, Hedley-Whyte ET. ALZHEIMER DISEASE DOES NOT PROTECT THE NEOSTRIATUM IN COMBINED CASES OF HUNTINGTON (HD) AND ALZHEIMER DISEASE (AD) Journal of Neuropathology and Experimental Neurology. 56: 617. DOI: 10.1097/00005072-199705000-00198  0.275
1991 Meissen GJ, Mastromauro CA, Kiely DK, McNamara DS, Myers RH. Understanding the decision to take the predictive test for Huntington disease. American Journal of Medical Genetics. 39: 404-10. PMID 1678928 DOI: 10.1002/Ajmg.1320390408  0.273
1987 Mastromauro C, Myers RH, Berkman B. Attitudes toward presymptomatic testing in Huntington disease. American Journal of Medical Genetics. 26: 271-82. PMID 2949611 DOI: 10.1002/Ajmg.1320260205  0.272
1996 Myers RH, Schaefer EJ, Wilson PW, D'Agostino R, Ordovas JM, Espino A, Au R, White RF, Knoefel JE, Cobb JL, McNulty KA, Beiser A, Wolf PA. Apolipoprotein E epsilon4 association with dementia in a population-based study: The Framingham study. Neurology. 46: 673-7. PMID 8618665 DOI: 10.1212/Wnl.46.3.673  0.271
1990 Doolittle TH, Myers RH, Lehrich JR, Birnbaum G, Sheremata W, Franklin GM, Nelson LM, Hauser SL. Multiple sclerosis sibling pairs: clustered onset and familial predisposition. Neurology. 40: 1546-52. PMID 2215946 DOI: 10.1212/Wnl.40.10.1546  0.27
2006 Kraja AT, Borecki IB, North K, Tang W, Myers RH, Hopkins PN, Arnett D, Corbett J, Adelman A, Province MA. Longitudinal and age trends of metabolic syndrome and its risk factors: the Family Heart Study. Nutrition & Metabolism. 3: 41. PMID 17147796 DOI: 10.1186/1743-7075-3-41  0.27
2002 Coady SA, Jaquish CE, Fabsitz RR, Larson MG, Cupples LA, Myers RH. Genetic variability of adult body mass index: a longitudinal assessment in framingham families. Obesity Research. 10: 675-81. PMID 12105290 DOI: 10.1038/Oby.2002.91  0.269
1986 Mastromauro C, Myers RH, Berkman B. Change in attitudes toward presymptomatic testing in Huntington disease. American Journal of Medical Genetics. 24: 369-71. PMID 3013007 DOI: 10.1002/Ajmg.1320240218  0.266
2002 Demissie S, Cupples LA, Myers R, Aliabadi P, Levy D, Felson DT. Genome scan for quantity of hand osteoarthritis: the Framingham Study. Arthritis and Rheumatism. 46: 946-52. PMID 11953971 DOI: 10.1002/Art.10149  0.266
1990 Myers RH, Kiely DK, Cupples LA, Kannel WB. Parental history is an independent risk factor for coronary artery disease: the Framingham Study. American Heart Journal. 120: 963-9. PMID 2220549 DOI: 10.1016/0002-8703(90)90216-K  0.266
1993 Sotrel A, Williams RS, Kaufmann WE, Myers RH. Evidence for neuronal degeneration and dendritic plasticity in cortical pyramidal neurons of Huntington's disease: a quantitative Golgi study. Neurology. 43: 2088-96. PMID 8413971 DOI: 10.1212/Wnl.43.10.2088  0.263
2001 O'Donnell CJ, Larson MG, Feng D, Sutherland PA, Lindpaintner K, Myers RH, D'Agostino RA, Levy D, Tofler GH. Genetic and environmental contributions to platelet aggregation: the Framingham heart study. Circulation. 103: 3051-6. PMID 11425767 DOI: 10.1161/01.Cir.103.25.3051  0.262
1997 Liao D, Myers R, Hunt S, Shahar E, Paton C, Burke G, Province M, Heiss G. Familial history of stroke and stroke risk. The Family Heart Study. Stroke. 28: 1908-12. PMID 9341694 DOI: 10.1161/01.Str.28.10.1908  0.261
1997 Taylor CA, Myers RH. Long-term impact of Huntington disease linkage testing. American Journal of Medical Genetics. 70: 365-70. PMID 9182776 DOI: 10.1002/(Sici)1096-8628(19970627)70:4<365::Aid-Ajmg7>3.0.Co;2-S  0.26
1991 Sotrel A, Paskevich PA, Kiely DK, Bird ED, Williams RS, Myers RH. Morphometric analysis of the prefrontal cortex in Huntington's disease. Neurology. 41: 1117-23. PMID 1829794 DOI: 10.1212/Wnl.41.7.1117  0.259
1997 Post WS, Larson MG, Myers RH, Galderisi M, Levy D. Heritability of left ventricular mass: the Framingham Heart Study. Hypertension. 30: 1025-8. PMID 9369250 DOI: 10.1161/01.Hyp.30.5.1025  0.257
1991 Vonsattel JP, Myers RH, Hedley-Whyte ET, Ropper AH, Bird ED, Richardson EP. Cerebral amyloid angiopathy without and with cerebral hemorrhages: a comparative histological study. Annals of Neurology. 30: 637-49. PMID 1763890 DOI: 10.1002/Ana.410300503  0.256
1992 Farrer LA, Myers RH, Cupples LA. Segregation analysis of total nevus density and estimation of lifetime risk and average onset age of melanoma. Cytogenetics and Cell Genetics. 59: 197-9. PMID 1737499 DOI: 10.1159/000133244  0.256
2005 Kraja AT, Hunt SC, Pankow JS, Myers RH, Heiss G, Lewis CE, Rao D, Province MA. An evaluation of the metabolic syndrome in the HyperGEN study. Nutrition & Metabolism. 2: 2. PMID 15656912 DOI: 10.1186/1743-7075-2-2  0.256
2002 Djoussé L, Myers RH, Province MA, Hunt SC, Eckfeldt JH, Evans G, Peacock JM, Ellison RC. Influence of apolipoprotein E, smoking, and alcohol intake on carotid atherosclerosis: National Heart, Lung, and Blood Institute Family Heart Study. Stroke; a Journal of Cerebral Circulation. 33: 1357-61. PMID 11988615 DOI: 10.1161/01.Str.0000014325.54063.1A  0.255
2003 Panhuysen CI, Cupples LA, Wilson PW, Herbert AG, Myers RH, Meigs JB. A genome scan for loci linked to quantitative insulin traits in persons without diabetes: the Framingham Offspring Study. Diabetologia. 46: 579-87. PMID 12739029 DOI: 10.1007/S00125-003-1066-Z  0.255
1999 Ellison RC, Myers RH, Zhang Y, Djoussé L, Knox S, Williams RR, Province MA. Effects of similarities in lifestyle habits on familial aggregation of high density lipoprotein and low density lipoprotein cholesterol: the NHLBI Family Heart Study. American Journal of Epidemiology. 150: 910-8. PMID 10547136 DOI: 10.1093/Oxfordjournals.Aje.A010099  0.254
1998 Farrer LA, Cupples LA, Myers RH, van Duijn CM, Mayeux R, Haines JL, Kukull WA, Hyman B, Pericak-Vance MA, Risch N. Effects of Age and Ethnicity on the Link Between APOE ϵ4 and Alzheimer Disease—Reply Jama. 279: 581. DOI: 10.1001/Jama.279.8.581A  0.253
2000 Hong Y, Leppert MF, Lin J, Hunt SC, Rich SS, Arnett DK, Myers RH, Eckfeldt J, Williams RR, Province MA. No evidence of linkage between the very-low-density lipoprotein receptor gene and fasting serum insulin or homeostasis model assessment insulin resistance index: the National Heart, Lung, and Blood Institute Family Heart Study. Metabolism: Clinical and Experimental. 49: 293-7. PMID 10726903 DOI: 10.1016/S0026-0495(00)90022-2  0.252
2010 Moser K, Biglan KM, Ross CA, Langbehn DR, Aylward E, Stout JC, Queller S, Carlozzi N, Duff K, Beglinger LJ, Paulsen JS, Tomusk A, Lifer S, Hastings S, Dawson J, ... ... Myers RH, et al. Inaugural Huntington Disease Clinical Research Symposium Organized by the Huntington Study Group Neurotherapeutics. 5: 202-212. DOI: 10.1016/J.Nurt.2007.10.053  0.252
1998 Nance MA, Seltzer W, Ashizawa T, Bennett R, McIntosh N, Myers RH, Potter NT, Shea DK. Laboratory Guidelines for Huntington Disease Genetic Testing The American Journal of Human Genetics. 62: 1243-1247. DOI: 10.1086/301846  0.251
2000 Djoussé L, Myers RH, Coon H, Arnett DK, Province MA, Ellison RC. Smoking influences the association between apolipoprotein E and lipids: the National Heart, Lung, and Blood Institute Family Heart Study. Lipids. 35: 827-31. PMID 10984105 DOI: 10.1007/S11745-000-0591-1  0.251
2013 Pichler I, Del Greco M. F, Gögele M, Lill CM, Bertram L, Do CB, Eriksson N, Foroud T, Myers RH, Nalls M, Keller MF, Benyamin B, Whitfield JB, Pramstaller PP, Hicks AA, et al. Correction: Serum Iron Levels and the Risk of Parkinson Disease: A Mendelian Randomization Study Plos Medicine. 10. DOI: 10.1371/Annotation/C4D81646-0C0E-4A3E-9425-B220Bae2D8B6  0.251
1999 Zhang Y, Kreger BE, Dorgan JF, Cupples LA, Myers RH, Splansky GL, Schatzkin A, Ellison RC. Parental age at child's birth and son's risk of prostate cancer. The Framingham Study. American Journal of Epidemiology. 150: 1208-12. PMID 10588081 DOI: 10.1093/Oxfordjournals.Aje.A009947  0.25
2000 Kronenberg F, Rich SS, Sholinsky P, Arnett DK, Province ME, Myers RH, Eckfeldt JH, Williams RR, Hunt SC. Insulin and hypertension in the NHLBI Family Heart Study: a sibpair approach to a controversial issue. American Journal of Hypertension. 13: 240-50. PMID 10777027 DOI: 10.1016/S0895-7061(99)00177-6  0.25
1992 Genest JJ, Martin-Munley SS, McNamara JR, Ordovas JM, Jenner J, Myers RH, Silberman SR, Wilson PW, Salem DN, Schaefer EJ. Familial lipoprotein disorders in patients with premature coronary artery disease. Circulation. 85: 2025-33. PMID 1534286 DOI: 10.1161/01.Cir.85.6.2025  0.243
1993 Cupples LA, Myers RH. Segregation analysis for high density lipoprotein in the Berkeley data. Genetic Epidemiology. 10: 629-34. PMID 8314072 DOI: 10.1002/Gepi.1370100650  0.242
1993 Myers RH, MacDonald ME, Koroshetz WJ, Duyao MP, Ambrose CM, Taylor SA, Barnes G, Srinidhi J, Lin CS, Whaley WL. De novo expansion of a (CAG)n repeat in sporadic Huntington's disease. Nature Genetics. 5: 168-73. PMID 8252042 DOI: 10.1038/ng1093-168  0.241
1993 Farrer LA, Cupples LA, Wiater P, Conneally PM, Gusella JF, Myers RH. The normal Huntington disease (HD) allele, or a closely linked gene, influences age at onset of HD. American Journal of Human Genetics. 53: 125-30. PMID 8317477  0.237
1979 Myers RH, Shafer DA. Hybrid ape offspring of a mating of gibbon and siamang. Science (New York, N.Y.). 205: 308-10. PMID 451603 DOI: 10.1126/Science.451603  0.237
1993 Kiely DK, Wolf PA, Cupples LA, Beiser AS, Myers RH. Familial aggregation of stroke. The Framingham Study. Stroke; a Journal of Cerebral Circulation. 24: 1366-71. PMID 8362432 DOI: 10.1161/01.Str.24.9.1366  0.236
2006 Franceschini N, Borecki IB, Gu CC, Heiss G, Province MA, Arnett DK, Lewis CE, Miller MB, Myers RH, Hunt SC, Freedman BI, North KE. Genotype-by-Sex Interaction on Fasting Insulin Levels: The Hypergen Study American Journal of Epidemiology. 163: S126-S126. DOI: 10.1093/Aje/163.Suppl_11.S126-C  0.235
2008 Assimes TL, Knowles JW, Priest JR, Basu A, Volcik KA, Southwick A, Tabor HK, Hartiala J, Allayee H, Grove ML, Tabibiazar R, Sidney S, Fortmann SP, Go A, Hlatky M, ... ... Myers R, et al. Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery disease. Human Genetics. 123: 399-408. PMID 18369664 DOI: 10.1007/S00439-008-0489-5  0.233
2008 MASSOOD T, LATOURELLE J, SRINIDHIMYSORE J, FOSSALE E, GILLIS T, GUSELLA J, MACDONALD M, MYERS R. HD Repeat Determines the Rate of Neuropathological Change Neurotherapeutics. 5: 367-367. DOI: 10.1016/J.Nurt.2007.10.013  0.229
2024 Koromina M, Ravi A, Panagiotaropoulou G, Schilder BM, Humphrey J, Braun A, Bidgeli T, Chatzinakos C, Coombes B, Kim J, Liu X, Terao C, O 'Connell KS, Adams M, Adolfsson R, ... ... Myers R, et al. Fine-mapping genomic loci refines bipolar disorder risk genes. Medrxiv : the Preprint Server For Health Sciences. PMID 38405768 DOI: 10.1101/2024.02.12.24302716  0.22
1994 Multani P, Myers RH, Blume HW, Schomer DL, Sotrel A. Neocortical dendritic pathology in human partial epilepsy: a quantitative Golgi study. Epilepsia. 35: 728-36. PMID 7521835 DOI: 10.1111/J.1528-1157.1994.Tb02503.X  0.22
2002 Baldwin CT, Cupples LA, Joost O, Demissie S, Chaisson C, Mcalindon T, Myers RH, Felson D. Absence of linkage or association for osteoarthritis with the vitamin D receptor/type II collagen locus: the Framingham Osteoarthritis Study. The Journal of Rheumatology. 29: 161-5. PMID 11824954  0.22
1983 Myers RH, Goldman D, Bird ED, Sax DS, Merril CR, Schoenfeld M, Wolf PA. Maternal transmission in Huntington's disease. Lancet. 1: 208-10. PMID 6130245 DOI: 10.1016/S0140-6736(83)92587-4  0.208
1992 Farrer LA, Cupples LA, Kiely DK, Conneally PM, Myers RH. Inverse relationship between age at onset of Huntington disease and paternal age suggests involvement of genetic imprinting. American Journal of Human Genetics. 50: 528-35. PMID 1531729  0.208
1989 Myers RH, Leavitt J, Farrer LA, Jagadeesh J, McFarlane H, Mastromauro CA, Mark RJ, Gusella JF. Homozygote for Huntington disease. American Journal of Human Genetics. 45: 615-8. PMID 2535231  0.206
1991 Myers RH, Sax DS, Koroshetz WJ, Mastromauro C, Cupples LA, Kiely DK, Pettengill FK, Bird ED. Factors associated with slow progression in Huntington's disease. Archives of Neurology. 48: 800-4. PMID 1832854 DOI: 10.1001/archneur.1991.00530200036015  0.203
1991 Farrer LA, Myers RH, Connor L, Cupples LA, Growdon JH. Segregation analysis reveals evidence of a major gene for Alzheimer disease. American Journal of Human Genetics. 48: 1026-33. PMID 2035523  0.201
1982 Myers RH, Madden JJ, Teague JL, Falek A. Factors related to onset age of Huntington disease. American Journal of Human Genetics. 34: 481-8. PMID 6211092  0.2
2008 Knowles JW, Assimes TL, Boerwinkle E, Fortmann SP, Go A, Grove ML, Hlatky M, Iribarren C, Li J, Myers R, Risch N, Sidney S, Southwick A, Volcik KA, Quertermous T. Failure to replicate an association of SNPs in the oxidized LDL receptor gene (OLR1) with CAD. Bmc Medical Genetics. 9: 23. PMID 18384690 DOI: 10.1186/1471-2350-9-23  0.199
1997 Farrer LA, Cupples LA, Haines JL, Hyman B, Kukull WA, Mayeux R, Myers RH, Pericak-Vance MA, Risch N, van Duijn CM. Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease. A meta-analysis. APOE and Alzheimer Disease Meta Analysis Consortium. Jama. 278: 1349-56. PMID 9343467  0.196
2003 McCarthy JJ, Lewitzky S, Reeves C, Permutt A, Glaser B, Groop LC, Lehner T, Meyer JM, Stram DO, Pearce CL, Bretsky P, Freedman M, Hirschhorn JN, Altshuler D, Kolonel LN, ... ... Myers RH, et al. Subject Index Vol. 55, 2003 Human Heredity. 55: 214-214. DOI: 10.1159/000074398  0.192
1977 Myers RH, De Castro JM. Learned aversions to intracerebral carbachol. Physiology & Behavior. 19: 467-72. PMID 613337 DOI: 10.1016/0031-9384(77)90219-0  0.192
2007 Litvan I, Halliday G, Hallett M, Goetz CG, Rocca W, Duyckaerts C, Ben-Shlomo Y, Dickson DW, Lang AE, Chesselet MF, Langston WJ, Di Monte DA, Gasser T, Hagg T, Hardy J, ... ... Myers RH, et al. The etiopathogenesis of Parkinson disease and suggestions for future research. Part I. Journal of Neuropathology and Experimental Neurology. 66: 251-7. PMID 17413315 DOI: 10.1097/nen.0b013e3180415e42  0.191
1992 Vonsattel JP, Myers RH, Bird ED, Ge P, Richardson EP. [Huntington disease: 7 cases with relatively preserved neostriatal islets]. Revue Neurologique. 148: 107-16. PMID 1534925  0.191
2005 Lin JP, Myers RH, Almasy L, Coon HH, Arnett DK, Hong Y, Hunt SC. Linkage of the cholesterol 7alpha-hydroxylase gene and low-density lipoprotein cholesterol conditional on apolipoprotein E association: the National Heart, Lung, and Blood Institute Family Heart Study. Chinese Medical Journal. 118: 362-9. PMID 15780204  0.186
2007 Basden A, Geng D, Guzman D, Morris T, Myers R, Saunter C. Shack-Hartmann sensor improvement using optical binning. Applied Optics. 46: 6136-41. PMID 17712378 DOI: 10.1364/Ao.46.006136  0.181
2002 Wagner GS, Maynard C, Andresen A, Anderson E, Myers R, Warner RA, Selvester RH. Evaluation of advanced electrocardiographic diagnostic software for detection of prior myocardial infarction. American Journal of Cardiology. 89: 75-79. PMID 11779530 DOI: 10.1016/S0002-9149(01)02170-1  0.179
2008 Takeuchi Y, Myers R, Danos O. Recombination and population mosaic of a multifunctional viral gene, adeno-associated virus cap. Plos One. 3: e1634. PMID 18286191 DOI: 10.1371/Journal.Pone.0001634  0.178
2010 Casto AM, Li JZ, Absher D, Myers R, Ramachandran S, Feldman MW. Characterization of X-linked SNP genotypic variation in globally distributed human populations. Genome Biology. 11: R10. PMID 20109212 DOI: 10.1186/Gb-2010-11-1-R10  0.176
2003 McCarthy JJ, Lewitzky S, Reeves C, Permutt A, Glaser B, Groop LC, Lehner T, Meyer JM, Stram DO, Pearce CL, Bretsky P, Freedman M, Hirschhorn JN, Altshuler D, Kolonel LN, ... ... Myers RH, et al. Contents Vol. 55, 2003 Human Heredity. 55: 215. DOI: 10.1159/000074399  0.171
1991 Cupples LA, Risch N, Farrer LA, Myers RH. Estimation of morbid risk and age at onset with missing information. American Journal of Human Genetics. 49: 76-87. PMID 1829582  0.164
2011 Rousset G, Gendron E, Myers R, Morris T. First star images corrected by multi-object adaptive optics Spie Newsroom. DOI: 10.1117/2.1201109.003736  0.164
2021 Volz E, Mishra S, Chand M, Barrett JC, Johnson R, Geidelberg L, Hinsley WR, Laydon DJ, Dabrera G, O'Toole Á, Amato R, Ragonnet-Cronin M, Harrison I, Jackson B, Ariani CV, ... ... Myers R, et al. Assessing transmissibility of SARS-CoV-2 lineage B.1.1.7 in England. Nature. PMID 33767447 DOI: 10.1038/s41586-021-03470-x  0.16
1985 Myers RH, Cupples LA, Schoenfeld M, D'Agostino RB, Terrin NC, Goldmakher N, Wolf PA. Maternal factors in onset of Huntington disease. American Journal of Human Genetics. 37: 511-23. PMID 3159258  0.159
2000 Myers RH. Genetic modifiers and predictive testing in Huntington's disease Neuroscience News. 3: 23-29.  0.157
2015 Jin L, Örvell C, Myers R, Rota PA, Nakayama T, Forcic D, Hiebert J, Brown KE. Genomic diversity of mumps virus and global distribution of the 12 genotypes. Reviews in Medical Virology. 25: 85-101. PMID 25424978 DOI: 10.1002/Rmv.1819  0.157
2015 Penedos AR, Myers R, Hadef B, Aladin F, Brown KE. Assessment of the Utility of Whole Genome Sequencing of Measles Virus in the Characterisation of Outbreaks. Plos One. 10: e0143081. PMID 26569100 DOI: 10.1371/journal.pone.0143081  0.157
1985 Myers RH, Schoenfeld M, Bird ED. Huntington's disease: genetics, chemical pathology, and management. Progress in Medical Genetics. 6: 91-122. PMID 2873625  0.155
2018 Aterido A, Cañete JD, Tornero J, Ferrándiz C, Pinto JA, Gratacós J, Queiró R, Montilla C, Torre-Alonso JC, Pérez-Venegas JJ, Fernández Nebro A, Muñoz-Fernández S, González CM, Roig D, Zarco P, ... ... Myers R, et al. Genetic variation at the glycosaminoglycan metabolism pathway contributes to the risk of psoriatic arthritis but not psoriasis. Annals of the Rheumatic Diseases. PMID 30552173 DOI: 10.1136/Annrheumdis-2018-214158  0.155
2021 Watson HJ, Thornton LM, Yilmaz Z, Baker JH, Coleman JRI, Adan RAH, Alfredsson L, Andreassen OA, Ask H, Berrettini WH, Boehnke M, Boehm I, Boni C, Buehren K, Bulant J, ... ... Myers R, et al. Common Genetic Variation and Age of Onset of Anorexia Nervosa. Biological Psychiatry Global Open Science. 2: 368-378. PMID 36324647 DOI: 10.1016/j.bpsgos.2021.09.001  0.151
1982 Myers RH, Growdon JH, Bird ED, Feldman RG, Martin JB. False-negative results with levodopa for early detection of Huntington's disease. The New England Journal of Medicine. 307: 561-2. PMID 6212764 DOI: 10.1056/NEJM198208263070922  0.15
2018 Wyllie DH, Sanderson N, Myers R, Peto T, Robinson E, Crook DW, Smith EG, Walker AS. Control of artefactual variation in reported inter-sample relatedness during clinical use of a sequencing pipeline. Journal of Clinical Microbiology. PMID 29875188 DOI: 10.1128/JCM.00104-18  0.146
1989 Haines JL, Farrer LA, Myers RH. Linkage map of anonymous loci near the CF gene. Progress in Clinical and Biological Research. 329: 29-34. PMID 2622958  0.145
2009 Hesselson SE, Matsson P, Shima JE, Fukushima H, Yee SW, Kobayashi Y, Gow JM, Ha C, Ma B, Poon A, Johns SJ, Stryke D, Castro RA, Tahara H, Choi JH, ... ... Myers R, et al. Genetic variation in the proximal promoter of ABC and SLC superfamilies: liver and kidney specific expression and promoter activity predict variation. Plos One. 4: e6942. PMID 19742321 DOI: 10.1371/Journal.Pone.0006942  0.139
2006 Myers R, Clark C, Khan A, Kellam P, Tedder R. Genotyping Hepatitis B virus from whole- and sub-genomic fragments using position-specific scoring matrices in HBV STAR. Journal of General Virology. 87: 1459-1464. PMID 16690910 DOI: 10.1099/Vir.0.81734-0  0.134
2004 Bartosch B, Stefanidis D, Myers R, Weiss R, Patience C, Takeuchi Y. Evidence and Consequence of Porcine Endogenous Retrovirus Recombination Journal of Virology. 78: 13880-13890. PMID 15564496 DOI: 10.1128/Jvi.78.24.13880-13890.2004  0.131
2022 Aggarwal D, Page AJ, Schaefer U, Savva GM, Myers R, Volz E, Ellaby N, Platt S, Groves N, Gallagher E, Tumelty NM, Le Viet T, Hughes GJ, Chen C, Turner C, et al. Genomic assessment of quarantine measures to prevent SARS-CoV-2 importation and transmission. Nature Communications. 13: 1012. PMID 35197443 DOI: 10.1038/s41467-022-28371-z  0.131
2022 McCrone JT, Hill V, Bajaj S, Pena RE, Lambert BC, Inward R, Bhatt S, Volz E, Ruis C, Dellicour S, Baele G, Zarebski AE, Sadilek A, Wu N, Schneider A, ... ... Myers R, et al. Context-specific emergence and growth of the SARS-CoV-2 Delta variant. Nature. PMID 35952712 DOI: 10.1038/s41586-022-05200-3  0.124
2023 Twohig KA, Harman K, Zaidi A, Aliabadi S, Nash SG, Sinnathamby M, Harrison I, Gallagher E, Groves N, Schwach F, Pearson C, Thornton A, Myers R, Chand M, Thelwall S, et al. Representativeness of whole-genome sequencing approaches in England: the importance for understanding inequalities associated with SARS-CoV-2 infection. Epidemiology and Infection. 151: e169. PMID 37726109 DOI: 10.1017/S0950268823001541  0.123
2012 Galiano M, Johnson BF, Myers R, Ellis J, Daniels R, Zambon M. Fatal cases of influenza A(H3N2) in children: insights from whole genome sequence analysis. Plos One. 7: e33166. PMID 22412998 DOI: 10.1371/journal.pone.0033166  0.123
2021 McCrone JT, Hill V, Bajaj S, Pena RE, Lambert BC, Inward R, Bhatt S, Volz E, Ruis C, Dellicour S, Baele G, Zarebski AE, Sadilek A, Wu N, Schneider A, ... ... Myers R, et al. Context-specific emergence and growth of the SARS-CoV-2 Delta variant. Medrxiv : the Preprint Server For Health Sciences. PMID 34981069 DOI: 10.1101/2021.12.14.21267606  0.118
1979 Myers RH, Falek A. Quantification of muscle tremor of Huntington's disease patients and their offspring in an early detection study. Biological Psychiatry. 14: 777-89. PMID 159079  0.117
2008 Cui A, Myers R, Xu W, Jin L. Analysis of the genetic variability of the mumps SH gene in viruses circulating in the UK between 1996 and 2005. Infection, Genetics and Evolution : Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases. 9: 71-80. PMID 19007915 DOI: 10.1016/j.meegid.2008.10.004  0.116
2022 Dabrera G, Allen H, Zaidi A, Flannagan J, Twohig K, Thelwall S, Marchant E, Aziz NA, Lamagni T, Myers R, Charlett A, Capelastegui F, Chudasama D, Clare T, Coukan F, et al. Assessment of mortality and hospital admissions associated with confirmed infection with SARS-CoV-2 Alpha variant: a matched cohort and time-to-event analysis, England, October to December 2020. Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin. 27. PMID 35593163 DOI: 10.2807/1560-7917.ES.2022.27.20.2100377  0.115
2022 Hill V, Du Plessis L, Peacock TP, Aggarwal D, Colquhoun R, Carabelli AM, Ellaby N, Gallagher E, Groves N, Jackson B, McCrone JT, O'Toole Á, Price A, Sanderson T, Scher E, ... ... Myers R, et al. The origins and molecular evolution of SARS-CoV-2 lineage B.1.1.7 in the UK. Virus Evolution. 8: veac080. PMID 36533153 DOI: 10.1093/ve/veac080  0.111
2023 O'Toole Á, Neher RA, Ndodo N, Borges V, Gannon B, Gomes JP, Groves N, King DJ, Maloney D, Lemey P, Lewandowski K, Loman N, Myers R, Omah IF, Suchard MA, et al. APOBEC3 deaminase editing in mpox virus as evidence for sustained human transmission since at least 2016. Science (New York, N.Y.). 382: 595-600. PMID 37917680 DOI: 10.1126/science.adg8116  0.108
2021 Aggarwal D, Myers R, Hamilton WL, Bharucha T, Tumelty NM, Brown CS, Meader EJ, Connor T, Smith DL, Bradley DT, Robson S, Bashton M, Shallcross L, Zambon M, Goodfellow I, et al. The role of viral genomics in understanding COVID-19 outbreaks in long-term care facilities. The Lancet. Microbe. PMID 34608459 DOI: 10.1016/S2666-5247(21)00208-1  0.105
2022 Nyberg T, Harman K, Zaidi A, Seaman SR, Andrews N, Nash SG, Charlett A, Lopez Bernal J, Myers R, Groves N, Gallagher E, Gharbia S, Chand M, Thelwall S, De Angelis D, et al. Hospitalisation and mortality risk for COVID-19 cases with SARS-CoV-2 AY.4.2 (VUI-21OCT-01) compared to non-AY.4.2 Delta variant sub-lineages. The Journal of Infectious Diseases. PMID 35184201 DOI: 10.1093/infdis/jiac063  0.093
2020 Manso CF, Bibby DF, Lythgow K, Mohamed H, Myers R, Williams D, Piorkowska R, Chan YT, Bowden R, Ansari MA, Ip CLC, Barnes E, Bradshaw D, Mbisa JL. Technical Validation of a Hepatitis C Virus Whole Genome Sequencing Assay for Detection of Genotype and Antiviral Resistance in the Clinical Pathway. Frontiers in Microbiology. 11: 576572. PMID 33162957 DOI: 10.3389/fmicb.2020.576572  0.092
2018 Dallman T, Ashton P, Schafer U, Jironkin A, Painset A, Shaaban S, Hartman H, Myers R, Underwood A, Jenkins C, Grant K. SnapperDB: A database solution for routine sequencing analysis of bacterial isolates. Bioinformatics (Oxford, England). PMID 29659710 DOI: 10.1093/bioinformatics/bty212  0.091
2011 Mandal S, Bradshaw L, Anderson LF, Brown T, Evans JT, Drobniewski F, Smith G, Magee JG, Barrett A, Blatchford O, Laurenson IF, Seagar AL, Ruddy M, White PL, Myers R, et al. Investigating transmission of Mycobacterium bovis in the United Kingdom in 2005 to 2008. Journal of Clinical Microbiology. 49: 1943-50. PMID 21430093 DOI: 10.1128/JCM.02299-10  0.091
2023 Hotta R, Pan W, Bhave S, Nagy N, Stavely R, Ohkura T, Krishnan K, de Couto G, Myers R, Rodriguez-Borlado L, Burns AJ, Goldstein AM. Isolation, Expansion, and Endoscopic Delivery of Autologous Enteric Neuronal Stem Cells in Swine. Cell Transplantation. 32: 9636897231215233. PMID 38049927 DOI: 10.1177/09636897231215233  0.091
2021 Lopez Bernal J, Andrews N, Gower C, Gallagher E, Simmons R, Thelwall S, Stowe J, Tessier E, Groves N, Dabrera G, Myers R, Campbell CNJ, Amirthalingam G, Edmunds M, Zambon M, et al. Effectiveness of Covid-19 Vaccines against the B.1.617.2 (Delta) Variant. The New England Journal of Medicine. PMID 34289274 DOI: 10.1056/NEJMoa2108891  0.091
2011 Kathiresan S, Reilly MP, Samani NJ, Schunkert H, Erdmann J, Assimes TL, Boerwinkle E, Hall A, Hengstenberg C, König IR, Laaksonen R, McPherson R, Thompson JR, Thorsteinsdottir U, Ziegler A, ... ... Myers R, et al. RANTES/CCL5 and risk for coronary events: Results from the MONICA/KORA Augsburg case-cohort, Athero-express and CARDIoGRAM studies Plos One. 6. DOI: 10.1371/journal.pone.0025734  0.085
2022 Aggarwal D, Warne B, Jahun AS, Hamilton WL, Fieldman T, du Plessis L, Hill V, Blane B, Watkins E, Wright E, Hall G, Ludden C, Myers R, Hosmillo M, Chaudhry Y, et al. Genomic epidemiology of SARS-CoV-2 in a UK university identifies dynamics of transmission. Nature Communications. 13: 751. PMID 35136068 DOI: 10.1038/s41467-021-27942-w  0.085
2022 Wyllie D, Do T, Myers R, Nikolayevskyy V, Crook D, Peto T, Alexander E, Robinson E, Walker AS, Campbell C, Smith EG. M. tuberculosis microvariation is common and is associated with transmission: analysis of three years prospective universal sequencing in England. The Journal of Infection. PMID 35595102 DOI: 10.1016/j.jinf.2022.05.011  0.084
2016 Thomson E, Ip CL, Badhan A, Christiansen MT, Adamson W, Ansari MA, Bibby D, Breuer J, Brown A, Bowden R, Bryant J, Bonsall D, Da Silva Filipe A, Hinds C, Hudson E, ... ... Myers R, et al. Comparison of next generation sequencing technologies for the comprehensive assessment of full-length hepatitis C viral genomes. Journal of Clinical Microbiology. PMID 27385709 DOI: 10.1128/JCM.00330-16  0.082
2023 Harman K, Nash SG, Webster HH, Groves N, Hardstaff J, Bridgen J, Blomquist PB, Hope R, Ashano E, Myers R, Rokadiya S, Hopkins S, Brown CS, Chand M, Dabrera G, et al. Comparison of the risk of hospitalisation among BA.1 and BA.2 COVID-19 cases treated with sotrovimab in the community in England. Influenza and Other Respiratory Viruses. 17: e13150. PMID 37246147 DOI: 10.1111/irv.13150  0.082
2013 Tedder RS, Bissett SL, Myers R, Ijaz S. The 'Red Queen' dilemma--running to stay in the same place: reflections on the evolutionary vector of HBV in humans. Antiviral Therapy. 18: 489-96. PMID 23792884 DOI: 10.3851/IMP2655  0.082
2013 Kim HJ, Myers R, Sihn CR, Rafizadeh S, Zhang XD. Slc26a6 functions as an electrogenic Cl-/HCO3- exchanger in cardiac myocytes. Cardiovascular Research. 100: 383-91. PMID 23933580 DOI: 10.1093/Cvr/Cvt195  0.08
2015 Myers R, Timofeyev V, Li N, Kim C, Ledford HA, Sirish P, Lau V, Zhang Y, Fayyaz K, Singapuri A, Lopez JE, Knowlton AA, Zhang XD, Chiamvimonvat N. Feedback Mechanisms for Cardiac-Specific microRNAs and cAMP Signaling in Electrical Remodeling. Circulation. Arrhythmia and Electrophysiology. PMID 25995211 DOI: 10.1161/Circep.114.002162  0.08
2004 Gale CV, Myers R, Tedder RS, Williams IG, Kellam P. Development of a novel human immunodeficiency virus type 1 subtyping tool, Subtype Analyzer (STAR): analysis of subtype distribution in London. Aids Research and Human Retroviruses. 20: 457-464. PMID 15186519 DOI: 10.1089/088922204323087697  0.079
2001 Lewis SL, Montgomery DC, Myers RH. Confidence interval coverage for designed experiments analyzed with GLMs Journal of Quality Technology. 33: 279-292. DOI: 10.1080/00224065.2001.11980079  0.072
2021 Lipworth S, Hough N, Weston N, Muller-Pebody B, Phin N, Myers R, Chapman S, Flight W, Alexander E, Smith EG, Robinson E, Peto TEA, Crook DW, Walker AS, Hopkins S, et al. Epidemiology of in England: an observational study. The Lancet. Microbe. 2: e498-e507. PMID 34632432 DOI: 10.1016/S2666-5247(21)00128-2  0.07
2021 Taylor H, Wall W, Ross D, Janarthanan R, Wang L, Aiano F, Ellis J, Gopal R, Andrews N, Patel M, Lackenby A, Myers R, Ramsay ME, Chow JY, Zambon M, et al. Cross sectional investigation of a COVID-19 outbreak at a London Army barracks: Neutralising antibodies and virus isolation. The Lancet Regional Health. Europe. 2: 100015. PMID 33870245 DOI: 10.1016/j.lanepe.2020.100015  0.069
2021 Tang S, Perez MS, Saavedra-Campos M, Paranthaman K, Myers R, Fok J, Crawley-Boevey E, Dun-Campbell K, Janarthanan R, Fernandez E, Vusirikala A, Patel B, Ma T, Amin-Chowdhury Z, Shetty N, et al. Mass testing after a single suspected or confirmed case of COVID-19 in London care homes, April-May 2020: implications for policy and practice. Age and Ageing. PMID 33620453 DOI: 10.1093/ageing/afab054  0.069
2010 Bakhos LL, Lockhart GR, Myers R, Linakis JG. Emergency department visits for concussion in young child athletes. Pediatrics. 126: e550-6. PMID 20805145 DOI: 10.1542/peds.2009-3101  0.065
2012 Glatter KA, Myers R, Chiamvimonvat N. Recommendations regarding dietary intake and caffeine and alcohol consumption in patients with cardiac arrhythmias: what do you tell your patients to do or not to do? Current Treatment Options in Cardiovascular Medicine. 14: 529-35. PMID 22865244 DOI: 10.1007/S11936-012-0193-6  0.064
2022 Andrews N, Tessier E, Stowe J, Gower C, Kirsebom F, Simmons R, Gallagher E, Thelwall S, Groves N, Dabrera G, Myers R, Campbell CNJ, Amirthalingam G, Edmunds M, Zambon M, et al. Duration of Protection against Mild and Severe Disease by Covid-19 Vaccines. The New England Journal of Medicine. PMID 35021002 DOI: 10.1056/NEJMoa2115481  0.061
2022 Andrews N, Stowe J, Kirsebom F, Toffa S, Rickeard T, Gallagher E, Gower C, Kall M, Groves N, O'Connell AM, Simons D, Blomquist PB, Zaidi A, Nash S, Iwani Binti Abdul Aziz N, ... ... Myers R, et al. Covid-19 Vaccine Effectiveness against the Omicron (B.1.1.529) Variant. The New England Journal of Medicine. PMID 35249272 DOI: 10.1056/NEJMoa2119451  0.061
2018 Fifer H, Cole M, Hughes G, Padfield S, Smolarchuk C, Woodford N, Wensley A, Mustafa N, Schaefer U, Myers R, Templeton K, Shepherd J, Underwood A. Sustained transmission of high-level azithromycin-resistant Neisseria gonorrhoeae in England: an observational study. The Lancet. Infectious Diseases. PMID 29523496 DOI: 10.1016/S1473-3099(18)30122-1  0.061
2019 Middleton BR, Talaugon S, Young TM, Wong L, Fluharty S, Reed K, Cosby C, Myers R. Bi-Directional Learning: Identifying Contaminants on the Yurok Indian Reservation. International Journal of Environmental Research and Public Health. 16. PMID 31547171 DOI: 10.3390/Ijerph16193513  0.061
2003 Andresen A, Gasperina MD, Myers R, Wagner GS, Warner RA, Selvester RH. An improved automated ECG algorithm for detecting acute and prior myocardial infarction. Journal of Electrocardiology. 105-10. PMID 12539106 DOI: 10.1054/jelc.2002.37162  0.06
2012 Baillie GJ, Galiano M, Agapow PM, Myers R, Chiam R, Gall A, Palser AL, Watson SJ, Hedge J, Underwood A, Platt S, McLean E, Pebody RG, Rambaut A, Green J, et al. Evolutionary dynamics of local pandemic H1N1/2009 influenza virus lineages revealed by whole-genome analysis. Journal of Virology. 86: 11-8. PMID 22013031 DOI: 10.1128/Jvi.05347-11  0.06
2004 Robinson TJ, Myers RH, Montgomery DC. Analysis considerations in industrial split-plot experiments with non-normal responses Journal of Quality Technology. 36: 180-192. DOI: 10.1080/00224065.2004.11980264  0.057
2021 Virginio C, Aldegheri L, Nola S, Brodbeck D, Brault L, Raveglia LF, Barilli A, Sabat M, Myers R. Identification of positive modulators of TRPM5 channel from a high-throughput screen using a fluorescent membrane potential assay. Slas Discovery : Advancing Life Sciences R & D. PMID 35058176 DOI: 10.1016/j.slasd.2021.10.004  0.057
1963 MYERS RH. Retinal detachment, associated with external exudative retinopathy and secondary glaucoma in a two year old child. The Journal of the Tennessee State Medical Association. Tennessee State Medical Association. 56: 285-6. PMID 13936968  0.056
2015 Harris TR, Bettaieb A, Kodani S, Dong H, Myers R, Chiamvimonvat N, Haj FG, Hammock BD. Inhibition of soluble epoxide hydrolase attenuates hepatic fibrosis and endoplasmic reticulum stress induced by carbon tetrachloride in mice. Toxicology and Applied Pharmacology. 286: 102-11. PMID 25827057 DOI: 10.1016/J.Taap.2015.03.022  0.055
2023 Hotta R, Rahman A, Bhave S, Stavely R, Pan W, Srinivasan S, de Couto G, Rodriguez-Borlado L, Myers R, Burns AJ, Goldstein AM. Transplanted ENSCs form functional connections with intestinal smooth muscle and restore colonic motility in nNOS-deficient mice. Stem Cell Research & Therapy. 14: 232. PMID 37667277 DOI: 10.1186/s13287-023-03469-3  0.053
2002 Borror CM, Montgomery DC, Myers RH. Evaluation of statistical designs for experiments involving noise variables Journal of Quality Technology. 34: 54-70. DOI: 10.1080/00224065.2002.11980129  0.053
2003 De la Fuente-Fernàndez R, Myers RH. A note of caution on correlation between sibling pairs [6] (multiple letters) Neurology. 60: 1561. PMID 12743265 DOI: 10.1212/WNL.60.9.1561  0.052
2009 Mello MJ, Myers R, Christian JB, Palmisciano L, Linakis JG. Injuries in youth football: national emergency department visits during 2001-2005 for young and adolescent players. Academic Emergency Medicine : Official Journal of the Society For Academic Emergency Medicine. 16: 243-8. PMID 19210487 DOI: 10.1111/j.1553-2712.2009.00357.x  0.052
2020 Ladhani SN, Chow JY, Janarthanan R, Fok J, Crawley-Boevey E, Vusirikala A, Fernandez E, Perez MS, Tang S, Dun-Campbell K, Evans EW, Bell A, Patel B, Amin-Chowdhury Z, Aiano F, ... ... Myers R, et al. Investigation of SARS-CoV-2 outbreaks in six care homes in London, April 2020. Eclinicalmedicine. 100533. PMID 32923993 DOI: 10.1016/j.eclinm.2020.100533  0.051
2011 Galiano M, Agapow PM, Thompson C, Platt S, Underwood A, Ellis J, Myers R, Green J, Zambon M. Evolutionary pathways of the pandemic influenza A (H1N1) 2009 in the UK. Plos One. 6: e23779. PMID 21887318 DOI: 10.1371/journal.pone.0023779  0.049
2014 Sivo G, Kulcsár C, Conan JM, Raynaud HF, Gendron E, Basden A, Vidal F, Morris T, Meimon S, Petit C, Gratadour D, Martin O, Hubert Z, Sevin A, Perret D, ... ... Myers R, et al. First on-sky SCAO validation of full LQG control with vibration mitigation on the CANARY pathfinder. Optics Express. 22: 23565-91. PMID 25321824 DOI: 10.1364/Oe.22.023565  0.048
1982 Birch JB, Myers RH. Robust analysis of covariance. Biometrics. 38: 699-713. PMID 6756495 DOI: 10.2307/2530050  0.045
2000 Kuhn AM, Myers RH, Carter WH. Incorporating noise factors into experiments with censored data Technometrics. 42: 376-383. DOI: 10.1080/00401706.2000.10485710  0.044
2012 Myers RH. Desires and normative truths: A holist's response to the sceptics Mind. 121: 375-406. DOI: 10.1093/mind/fzs068  0.042
1999 Lewis SL, Montgomery DC, Myers RH. The analysis of designed experiments with non-normal responses Quality Engineering. 12: 225-243. DOI: 10.1080/08982119908962580  0.042
2001 Lewis SL, Montgomery DC, Myers RH. Examples of designed experiments with nonnormal responses Journal of Quality Technology. 33: 265-278. DOI: 10.1080/00224065.2001.11980078  0.042
2018 Mbisa JL, Kirwan P, Tostevin A, Ledesma J, Bibby DF, Brown A, Myers R, Hassan AS, Murphy G, Asboe D, Pozniak A, Kirk S, Gill ON, Sabin C, Delpech V, et al. Determining the origins of HIV-1 drug-resistant minority variants in people who are recently infected using phylogenetic reconstruction. Clinical Infectious Diseases : An Official Publication of the Infectious Diseases Society of America. PMID 30534981 DOI: 10.1093/Cid/Ciy1048  0.042
2014 Haagmans BL, Al Dhahiry SH, Reusken CB, Raj VS, Galiano M, Myers R, Godeke GJ, Jonges M, Farag E, Diab A, Ghobashy H, Alhajri F, Al-Thani M, Al-Marri SA, Al Romaihi HE, et al. Middle East respiratory syndrome coronavirus in dromedary camels: an outbreak investigation. The Lancet. Infectious Diseases. 14: 140-5. PMID 24355866 DOI: 10.1016/S1473-3099(13)70690-X  0.04
2014 Benitez A, Yuan F, Nakajima S, Wei L, Qian L, Myers R, Hu JJ, Lan L, Zhang Y. Damage-dependent regulation of MUS81-EME1 by Fanconi anemia complementation group A protein. Nucleic Acids Research. 42: 1671-83. PMID 24170812 DOI: 10.1093/Nar/Gkt975  0.04
2004 Robinson TJ, Borror CM, Myers RH. Robust parameter design: A review Quality and Reliability Engineering International. 20: 81-101. DOI: 10.1002/Qre.602  0.04
2020 Ladhani SN, Chow JY, Janarthanan R, Fok J, Crawley-Boevey E, Vusirikala A, Fernandez E, Perez MS, Tang S, Dun-Campbell K, Evans EW, Bell A, Patel B, Amin-Chowdhury Z, Aiano F, ... ... Myers R, et al. INCREASED RISK OF SARS-CoV-2 INFECTION IN STAFF WORKING ACROSS DIFFERENT CARE HOMES ENCHANCED CoVID-19 OUTBREAK INVESTIGATIONS IN LONDON CARE HOMES. The Journal of Infection. PMID 32735893 DOI: 10.1016/j.jinf.2020.07.027  0.04
2021 Barilli A, Aldegheri L, Bianchi F, Brault L, Brodbeck D, Castelletti L, Feriani A, Lingard I, Myers R, Nola S, Piccoli L, Pompilio D, Raveglia LF, Salvagno C, Tassini S, et al. From High-Throughput Screening to Target Validation: Benzo[]isothiazoles as Potent and Selective Agonists of Human Transient Receptor Potential Cation Channel Subfamily M Member 5 Possessing In Vivo Gastrointestinal Prokinetic Activity in Rodents. Journal of Medicinal Chemistry. PMID 33890770 DOI: 10.1021/acs.jmedchem.1c00065  0.039
2024 Cogdale J, Kele B, Myers R, Harvey R, Lofts A, Mikaiel T, Hoschler K, Banyard AC, James J, Mollett BC, Byrne AM, Lopez-Bernal J, Watson CH, Chand M, Welfare W, et al. A case of swine influenza A(H1N2)v in England, November 2023. Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin. 29. PMID 38240057 DOI: 10.2807/1560-7917.ES.2024.29.3.2400002  0.039
2007 Zaitseva L, Myers R, Fassati A. tRNAs promote nuclear import of HIV-1 intracellular reverse transcription complexes. Plos Biology. 4: e332. PMID 17020411 DOI: 10.1371/journal.pbio.0040332  0.038
1996 Myers WR, Myers RH, Carter WH, White KL. Two-stage designs for the logistic regression model in single-agent bioassays. Journal of Biopharmaceutical Statistics. 6: 283-301. PMID 8854233 DOI: 10.1080/10543409608835144  0.037
2006 Wang Y, Myers RH, Smith EP, Ye K. D-optimal designs for Poisson regression models Journal of Statistical Planning and Inference. 136: 2831-2845. DOI: 10.1016/J.Jspi.2004.10.017  0.036
2006 Liang L, Anderson-Cook CM, Robinson TJ, Myers RH. Three-dimensional variance dispersion graphs for split-plot designs Journal of Computational and Graphical Statistics. 15: 757-778. DOI: 10.1198/106186006X157117  0.036
2023 Billipp TE, Fung C, Webeck LM, Sargent DB, Gologorsky MB, McDaniel MM, Kasal DN, McGinty JW, Barrow KA, Rich LM, Barilli A, Sabat M, Debley JS, Myers R, Howitt MR, et al. Tuft cell-derived acetylcholine regulates epithelial fluid secretion. Biorxiv : the Preprint Server For Biology. PMID 36993541 DOI: 10.1101/2023.03.17.533208  0.035
2012 Osborn J, De Cos Juez FJ, Guzman D, Butterley T, Myers R, Guesalaga A, Laine J. Using artificial neural networks for open-loop tomography. Optics Express. 20: 2420-34. PMID 22330480 DOI: 10.1364/OE.20.002420  0.035
2003 Zahran A, Anderson-Cook CM, Myers RH, Smith EP. Modifying 22 factorial designs to accommodate a restricted design space Journal of Quality Technology. 35: 387-392. DOI: 10.1080/00224065.2003.11980236  0.035
2011 Basden A, Geng D, Myers R, Younger E. Durham adaptive optics real-time controller. Applied Optics. 49: 6354-63. PMID 21068868 DOI: 10.1364/AO.49.006354  0.034
2021 Jeffery-Smith A, Dun-Campbell K, Janarthanan R, Fok J, Crawley-Boevey E, Vusirikala A, Fernandez Ruiz De Olano E, Sanchez Perez M, Tang S, Rowland TA, Wynne-Evans E, Bell A, Patel B, Amin-Chowdhury Z, Aiano F, ... ... Myers R, et al. Infection and transmission of SARS-CoV-2 in London care homes reporting no cases or outbreaks of COVID-19: Prospective observational cohort study, England 2020. The Lancet Regional Health. Europe. 3: 100038. PMID 33870248 DOI: 10.1016/j.lanepe.2021.100038  0.034
2005 Montgomery DC, Myers RH, Carter WH, Vining GG. The hierarchy principle in designed industrial experiments Quality and Reliability Engineering International. 21: 197-201. DOI: 10.1002/Qre.615  0.033
1959 MYERS RH. An unusual case of spontaneous hemorrhage into the primary vitreous of nine-month-old child. The Journal of the Tennessee State Medical Association. Tennessee State Medical Association. 52: 448-9. PMID 14425609  0.033
2017 Myers R, Kim H, Hsieh AH, O'Toole RV, Sciadini MF. When Should We Change Drill Bits? A Mechanical Comparison of New, Reprocessed, and Damaged Bits. Journal of Orthopaedic Trauma. PMID 28166171 DOI: 10.1097/Bot.0000000000000812  0.033
2012 Myers RH. Relations across the Taiwan Strait: The current détente and its limits Charting China's Future: Domestic and International Challanges. 127-139. DOI: 10.4324/9780203817421  0.032
2004 Myers RH. Finding value in Davidson Canadian Journal of Philosophy. 34: 107-136.  0.032
2005 Chain BM, Myers R. Variability and conservation in hepatitis B virus core protein. Bmc Microbiology. 5: 33. PMID 15921513 DOI: 10.1186/1471-2180-5-33  0.03
2005 Myers WR, Brenneman WA, Myers RH. A dual-response approach to robust parameter design for a generalized linear model Journal of Quality Technology. 37: 130-138. DOI: 10.1080/00224065.2005.11980311  0.029
2021 Ruan Z, Haley E, Orozco IJ, Sabat M, Myers R, Roth R, Du J, Lü W. Structures of the TRPM5 channel elucidate mechanisms of activation and inhibition. Nature Structural & Molecular Biology. PMID 34168372 DOI: 10.1038/s41594-021-00607-4  0.026
2012 Onyango CO, Welch SR, Munywoki PK, Agoti CN, Bett A, Ngama M, Myers R, Cane PA, Nokes DJ. Molecular epidemiology of human rhinovirus infections in Kilifi, coastal Kenya. Journal of Medical Virology. 84: 823-31. PMID 22431032 DOI: 10.1002/jmv.23251  0.026
1990 Gennings C, Dawson KS, Carter WH, Myers RH. Interpreting plots of a multidimensional dose-response surface in a parallel coordinate system. Biometrics. 46: 719-35. PMID 2242411 DOI: 10.2307/2532091  0.026
1998 Metzger TA, Myers RH. Chinese nationalism and American policy Orbis. 42: 21-36.  0.026
2012 Franc BL, Myers R, Pounds TR, Bolton G, Conte F, Bartheld M, Da Silva AJ. Clinical utility of SPECT-(low-dose)CT versus SPECT alone in patients presenting for bone scintigraphy. Clinical Nuclear Medicine. 37: 26-34. PMID 22157024 DOI: 10.1097/RLU.0b013e3182392bd0  0.023
2010 Guzmán D, Juez FJ, Myers R, Guesalaga A, Lasheras FS. Modeling a MEMS deformable mirror using non-parametric estimation techniques. Optics Express. 18: 21356-69. PMID 20941032  0.021
1958 MYERS RH. Present relationship between ophthalmology and optometry. Rocky Mountain Medical Journal. 55: 41-4. PMID 13555611  0.021
2012 Andersson MI, Low N, Irish CJ, Carrington D, Hickman M, Myers R, Teo CG, Ijaz S. Molecular epidemiology of a large community-based outbreak of hepatitis B in Bristol, U.K. Journal of Clinical Virology : the Official Publication of the Pan American Society For Clinical Virology. 53: 125-9. PMID 22079304 DOI: 10.1016/j.jcv.2011.10.012  0.021
2000 Diamond L, Myers RH. Elections and democracy in greater China China Quarterly. 365-386.  0.02
1999 Myers RH. Response surface methodology - Current status and future directions Journal of Quality Technology. 31: 30-44.  0.019
2000 Chao L, Myers RH. How elections promoted democracy in Taiwan under martial law China Quarterly. 387-409.  0.019
2022 Videtich K, Moran K, Zajac L, Myers R. Changing the trajectory of clinical precepting for nurse practitioner students with the development of a preceptor resource network. Journal of the American Association of Nurse Practitioners. PMID 35622382 DOI: 10.1097/JXX.0000000000000732  0.018
1958 MYERS RH. Vascular changes in the eyes of diabetic patients. The Journal of the Tennessee State Medical Association. Tennessee State Medical Association. 51: 90-3. PMID 13514795  0.018
1969 Ott RL, Myers RH. Experimental designs for estimating effective doses. Clinical Pharmacology and Therapeutics. 10: 207-12. PMID 5775987 DOI: 10.1002/Cpt1969102207  0.018
1948 MYERS RH. Importance of early diagnosis and treatment of strabismus. Memphis Medical Journal. 23: 120-4. PMID 18872015  0.018
2000 Lin H, Myers RH, Ye K. Bayesian two-stage optimal design for mixture models Journal of Statistical Computation and Simulation. 66: 209-231.  0.018
2012 Myers RH, Montgomery DC, Vining GG, Robinson TJ. Generalized Linear Models: With Applications in Engineering and the Sciences: Second Edition Generalized Linear Models: With Applications in Engineering and the Sciences: Second Edition. 1-505. DOI: 10.1002/9780470556986  0.014
1999 Jensen DR, Myers RH. Second-order designs in two stages Biometrical Journal. 41: 931-942.  0.014
2010 Guzmán D, Juez FJ, Lasheras FS, Myers R, Young L. Deformable mirror model for open-loop adaptive optics using multivariate adaptive regression splines. Optics Express. 18: 6492-505. PMID 20389672 DOI: 10.1364/OE.18.006492  0.012
2011 Myers RH. Cooperating to promote the good Analyse Und Kritik. 2011: 123-140.  0.012
2016 Cunningham E, Chan YT, Aghaizu A, Bibby DF, Murphy G, Tosswill J, Harris RJ, Myers R, Field N, Delpech V, Cane PA, Gill ON, Mbisa JL. Enhanced surveillance of HIV-1 drug resistance in recently infected MSM in the UK. The Journal of Antimicrobial Chemotherapy. PMID 27742812 DOI: 10.1093/jac/dkw404  0.012
1966 Myers RH. The speakers' platform: neglected medium. National Conference On Dental Public Relations. 2: 1101-9. PMID 4381431  0.011
2007 Basden A, Butterley T, Myers R, Wilson R. Durham extremely large telescope adaptive optics simulation platform. Applied Optics. 46: 1089-98. PMID 17304307 DOI: 10.1364/ao.46.001089  0.011
2004 Myers RH, Montgomery DC, Geoffrey Vining G, Borror CM, Kowalski SM. Response Surface Methodology: A Retrospective and Literature Survey Journal of Quality Technology. 36: 53-78.  0.01
2021 Ruan Z, Haley E, Orozco IJ, Sabat M, Myers R, Roth R, Du J, Lü W. Author Correction: Structures of the TRPM5 channel elucidate mechanisms of activation and inhibition. Nature Structural & Molecular Biology. PMID 34285419 DOI: 10.1038/s41594-021-00641-2  0.01
2020 Demirjian A, Singh C, Tebruegge M, Herbert R, Draz N, Mirfenderesky M, Jones V, Hinstridge P, Seneviratne R, Myers R, Ellis J, Miah S, Meadows CI, Kenny J, Alonso A, et al. Probable Vertical Transmission of SARS-CoV-2 Infection. The Pediatric Infectious Disease Journal. PMID 32658096 DOI: 10.1097/INF.0000000000002821  0.01
2016 Myers R, Betz JM, Bøjstrup M, Craft NE, Figore H, Hall A, Joseph G, Kennedy D, Khachik F, Mudge E, Phillips MM, Phillips T, Richards LD, Rimmer CA, Schaneberg BT, et al. AOAC SMPR(®) 2016.004. Journal of Aoac International. 99: 1105-6. PMID 27455940 DOI: 10.5740/Jaoacint.Smpr2016.004  0.01
2012 Kuo TC, Myers RH. Taiwan’s economic transformation: Leadership, property rights and institutional change 1949–1965 Taiwan's Economic Transformation: Leadership, Property Rights and Institutional Change 1949-1965. 1-164. DOI: 10.4324/9780203808016  0.01
2011 Myers RH. Self-Governance and Cooperation Self-Governance and Cooperation. 1-190. DOI: 10.1093/acprof:oso/9780199256594.001.0001  0.01
2011 Myers RH. Reply to anton leist. Keeping constructivism in its place Analyse Und Kritik. 2011: 149-153.  0.01
2011 Sebastiani P, Solovieff N, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Perls TT. Retraction (Science) Science. 333: 404.  0.01
2003 Zahran A, Anderson-Cook CM, Myers RH. Fraction of design space to assess prediction capability of response surface designs Journal of Quality Technology. 35: 377-386. DOI: 10.1080/00224065.2003.11980235  0.01
2001 Myers RH, Petersen LC. Privacy rules under the Gramm-Leach-Bliley Act and HIPAA. Managed Care Interface. 14: 74-7. PMID 11569310  0.01
1993 Myers RH, MacDonald ME, Gusella JF. Discrepancy resolved. Nature Genetics. 5: 215. PMID 8110292 DOI: 10.1038/ng1193-215b  0.01
1967 Grizzard HT, Myers RH. An unusual cause of ocular pain. Journal of the Tennessee Medical Association. 60: 1332-3. PMID 6079119  0.01
1964 DESAUSSURE RL, MYERS RH, SIMMONS JC. CAROTID CAVERNOUS FISTULA. Journal of the Tennessee Medical Association. 57: 91-4. PMID 14135606  0.01
1954 MYERS RH. Surgery of the inferior oblique. The Journal of the Tennessee State Medical Association. Tennessee State Medical Association. 47: 412-5. PMID 13202182  0.01
1953 MYERS RH. Duane retraction syndrome: a strabismus problem. Southern Medical Journal. 46: 720. PMID 13076796  0.01
1951 MYERS RH. The child with a squint. The Journal of Pediatrics. 39: 516-8. PMID 14881053  0.01
1950 MYERS RH. Revaluation of the snare technique for enucleation. American Journal of Ophthalmology. 33: 1143-4. PMID 15425614  0.01
1949 MYERS RH. Ectropion left upper eyelid corrected by skin graft; hair graft to left brow and correction of left monocular convergent strabismus. Memphis Medical Journal. 24: 115. PMID 18145663  0.01
1946 MYERS RH. Acute trachoma treated with sulfanilamide. Memphis Medical Journal. 21: 140. PMID 20999742  0.01
1945 MYERS RH. Thrombosis of retinal vein treated with dicumarol. American Journal of Ophthalmology. 28: 1374. PMID 21006578  0.01
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